ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: Loss of function effect and plausibility of a dominant negative mechanism

Emanuele Panza, Juan M. Escamilla-Honrubia, Clara Marco-Marín, Nadine Gougeard, Giuseppe De Michele, Vincenzo Brescia Morra, Rocco Liguori, Leonardo Salviati, Maria Alice Donati, Roberto Cusano, Tommaso Pippucci, Roberto Ravazzolo, Andrea H. Németh, Sarah Smithson, Sally Davies, Jane A. Hurst, Domenico Bordo, Vicente Rubio, Marco Seri

Research output: Contribution to journalLetter

Original languageEnglish
Article numbere3
JournalBrain
Volume139
Issue number1
DOIs
Publication statusPublished - Jan 1 2016

ASJC Scopus subject areas

  • Clinical Neurology

Cite this

Panza, E., Escamilla-Honrubia, J. M., Marco-Marín, C., Gougeard, N., De Michele, G., Morra, V. B., ... Seri, M. (2016). ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: Loss of function effect and plausibility of a dominant negative mechanism. Brain, 139(1), [e3]. https://doi.org/10.1093/brain/awv247

ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9 : Loss of function effect and plausibility of a dominant negative mechanism. / Panza, Emanuele; Escamilla-Honrubia, Juan M.; Marco-Marín, Clara; Gougeard, Nadine; De Michele, Giuseppe; Morra, Vincenzo Brescia; Liguori, Rocco; Salviati, Leonardo; Donati, Maria Alice; Cusano, Roberto; Pippucci, Tommaso; Ravazzolo, Roberto; Németh, Andrea H.; Smithson, Sarah; Davies, Sally; Hurst, Jane A.; Bordo, Domenico; Rubio, Vicente; Seri, Marco.

In: Brain, Vol. 139, No. 1, e3, 01.01.2016.

Research output: Contribution to journalLetter

Panza, E, Escamilla-Honrubia, JM, Marco-Marín, C, Gougeard, N, De Michele, G, Morra, VB, Liguori, R, Salviati, L, Donati, MA, Cusano, R, Pippucci, T, Ravazzolo, R, Németh, AH, Smithson, S, Davies, S, Hurst, JA, Bordo, D, Rubio, V & Seri, M 2016, 'ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: Loss of function effect and plausibility of a dominant negative mechanism', Brain, vol. 139, no. 1, e3. https://doi.org/10.1093/brain/awv247
Panza, Emanuele ; Escamilla-Honrubia, Juan M. ; Marco-Marín, Clara ; Gougeard, Nadine ; De Michele, Giuseppe ; Morra, Vincenzo Brescia ; Liguori, Rocco ; Salviati, Leonardo ; Donati, Maria Alice ; Cusano, Roberto ; Pippucci, Tommaso ; Ravazzolo, Roberto ; Németh, Andrea H. ; Smithson, Sarah ; Davies, Sally ; Hurst, Jane A. ; Bordo, Domenico ; Rubio, Vicente ; Seri, Marco. / ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9 : Loss of function effect and plausibility of a dominant negative mechanism. In: Brain. 2016 ; Vol. 139, No. 1.
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AU - Gougeard, Nadine

AU - De Michele, Giuseppe

AU - Morra, Vincenzo Brescia

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