Erratum: Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760))

Claire Angebault; Pierre Olivier Guichet; Yasmina Talmat-Amar; Majida Charif; Sylvie Gerber; Lucas Fares-Taie; Naig Gueguen; François Halloy; David Moore; Patrizia Amati-Bonneau; Gael Manes; Maxime Hebrard; Béatrice Bocquet; Mélanie Quiles; Camille Piro-Mégy; Marisa Teigell; Cécile Delettre; Mireille Rossel; Isabelle Meunier; Markus Preising; Birgit Lorenz; Valerio Carelli; Patrick F. Chinnery; Patrick Yu-Wai-Man; Josseline Kaplan; Agathe Roubertie; Abdelhamid Barakat; Dominique Bonneau; Pascal Reynier; Jean Michel Rozet; Pascale Bomont; Christian P. Hamel; Guy Lenaers

doi:10.1016/j.ajhg.2015.10.015

Erratum: Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760))

Claire Angebault, Pierre Olivier Guichet, Yasmina Talmat-Amar, Majida Charif, Sylvie Gerber, Lucas Fares-Taie, Naig Gueguen, François Halloy, David Moore, Patrizia Amati-Bonneau, Gael Manes, Maxime Hebrard, Béatrice Bocquet, Mélanie Quiles, Camille Piro-Mégy, Marisa Teigell, Cécile Delettre, Mireille Rossel, Isabelle Meunier, Markus PreisingBirgit Lorenz, Valerio Carelli, Patrick F. Chinnery, Patrick Yu-Wai-Man, Josseline Kaplan, Agathe Roubertie, Abdelhamid Barakat, Dominique Bonneau, Pascal Reynier, Jean Michel Rozet, Pascale Bomont, Christian P. Hamel, Guy Lenaers

Istituto Scienze Neurologiche

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	769
Number of pages	1
Journal	American Journal of Human Genetics
Volume	97
Issue number	5
DOIs	https://doi.org/10.1016/j.ajhg.2015.10.015
Publication status	Published - Nov 5 2015

ASJC Scopus subject areas

Genetics
Genetics(clinical)

Access to Document

10.1016/j.ajhg.2015.10.015

Cite this

Angebault, C., Guichet, P. O., Talmat-Amar, Y., Charif, M., Gerber, S., Fares-Taie, L., Gueguen, N., Halloy, F., Moore, D., Amati-Bonneau, P., Manes, G., Hebrard, M., Bocquet, B., Quiles, M., Piro-Mégy, C., Teigell, M., Delettre, C., Rossel, M., Meunier, I., ... Lenaers, G. (2015). Erratum: Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760)). American Journal of Human Genetics, 97(5), 769. https://doi.org/10.1016/j.ajhg.2015.10.015

Erratum : Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760)). / Angebault, Claire; Guichet, Pierre Olivier; Talmat-Amar, Yasmina; Charif, Majida; Gerber, Sylvie; Fares-Taie, Lucas; Gueguen, Naig; Halloy, François; Moore, David; Amati-Bonneau, Patrizia; Manes, Gael; Hebrard, Maxime; Bocquet, Béatrice; Quiles, Mélanie; Piro-Mégy, Camille; Teigell, Marisa; Delettre, Cécile; Rossel, Mireille; Meunier, Isabelle; Preising, Markus; Lorenz, Birgit; Carelli, Valerio; Chinnery, Patrick F.; Yu-Wai-Man, Patrick; Kaplan, Josseline; Roubertie, Agathe; Barakat, Abdelhamid; Bonneau, Dominique; Reynier, Pascal; Rozet, Jean Michel; Bomont, Pascale; Hamel, Christian P.; Lenaers, Guy.

In: American Journal of Human Genetics, Vol. 97, No. 5, 05.11.2015, p. 769.

Research output: Contribution to journal › Article

Angebault, C, Guichet, PO, Talmat-Amar, Y, Charif, M, Gerber, S, Fares-Taie, L, Gueguen, N, Halloy, F, Moore, D, Amati-Bonneau, P, Manes, G, Hebrard, M, Bocquet, B, Quiles, M, Piro-Mégy, C, Teigell, M, Delettre, C, Rossel, M, Meunier, I, Preising, M, Lorenz, B, Carelli, V, Chinnery, PF, Yu-Wai-Man, P, Kaplan, J, Roubertie, A, Barakat, A, Bonneau, D, Reynier, P, Rozet, JM, Bomont, P, Hamel, CP & Lenaers, G 2015, 'Erratum: Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760))', American Journal of Human Genetics, vol. 97, no. 5, pp. 769. https://doi.org/10.1016/j.ajhg.2015.10.015

Angebault, Claire ; Guichet, Pierre Olivier ; Talmat-Amar, Yasmina ; Charif, Majida ; Gerber, Sylvie ; Fares-Taie, Lucas ; Gueguen, Naig ; Halloy, François ; Moore, David ; Amati-Bonneau, Patrizia ; Manes, Gael ; Hebrard, Maxime ; Bocquet, Béatrice ; Quiles, Mélanie ; Piro-Mégy, Camille ; Teigell, Marisa ; Delettre, Cécile ; Rossel, Mireille ; Meunier, Isabelle ; Preising, Markus ; Lorenz, Birgit ; Carelli, Valerio ; Chinnery, Patrick F. ; Yu-Wai-Man, Patrick ; Kaplan, Josseline ; Roubertie, Agathe ; Barakat, Abdelhamid ; Bonneau, Dominique ; Reynier, Pascal ; Rozet, Jean Michel ; Bomont, Pascale ; Hamel, Christian P. ; Lenaers, Guy. / Erratum : Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760)). In: American Journal of Human Genetics. 2015 ; Vol. 97, No. 5. pp. 769.

@article{7d6293d5fee3449d9537f5f64b3e0d14,

title = "Erratum: Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760))",

author = "Claire Angebault and Guichet, {Pierre Olivier} and Yasmina Talmat-Amar and Majida Charif and Sylvie Gerber and Lucas Fares-Taie and Naig Gueguen and Fran{\c c}ois Halloy and David Moore and Patrizia Amati-Bonneau and Gael Manes and Maxime Hebrard and B{\'e}atrice Bocquet and M{\'e}lanie Quiles and Camille Piro-M{\'e}gy and Marisa Teigell and C{\'e}cile Delettre and Mireille Rossel and Isabelle Meunier and Markus Preising and Birgit Lorenz and Valerio Carelli and Chinnery, {Patrick F.} and Patrick Yu-Wai-Man and Josseline Kaplan and Agathe Roubertie and Abdelhamid Barakat and Dominique Bonneau and Pascal Reynier and Rozet, {Jean Michel} and Pascale Bomont and Hamel, {Christian P.} and Guy Lenaers",

year = "2015",

month = nov,

day = "5",

doi = "10.1016/j.ajhg.2015.10.015",

language = "English",

volume = "97",

pages = "769",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "5",

}

TY - JOUR

T1 - Erratum

T2 - Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760))

AU - Angebault, Claire

AU - Guichet, Pierre Olivier

AU - Talmat-Amar, Yasmina

AU - Charif, Majida

AU - Gerber, Sylvie

AU - Fares-Taie, Lucas

AU - Gueguen, Naig

AU - Halloy, François

AU - Moore, David

AU - Amati-Bonneau, Patrizia

AU - Manes, Gael

AU - Hebrard, Maxime

AU - Bocquet, Béatrice

AU - Quiles, Mélanie

AU - Piro-Mégy, Camille

AU - Teigell, Marisa

AU - Delettre, Cécile

AU - Rossel, Mireille

AU - Meunier, Isabelle

AU - Preising, Markus

AU - Lorenz, Birgit

AU - Carelli, Valerio

AU - Chinnery, Patrick F.

AU - Yu-Wai-Man, Patrick

AU - Kaplan, Josseline

AU - Roubertie, Agathe

AU - Barakat, Abdelhamid

AU - Bonneau, Dominique

AU - Reynier, Pascal

AU - Rozet, Jean Michel

AU - Bomont, Pascale

AU - Hamel, Christian P.

AU - Lenaers, Guy

PY - 2015/11/5

Y1 - 2015/11/5

UR - http://www.scopus.com/inward/record.url?scp=84947908961&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84947908961&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2015.10.015

DO - 10.1016/j.ajhg.2015.10.015

M3 - Article

AN - SCOPUS:84947908961

VL - 97

SP - 769

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

SN - 0002-9297

IS - 5

ER -