Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease

D. Pareyson; D. Menichella; S. Botti; A. Sghirlanzoni; E. Fallica; M. Mora; C. Ciano; M. E. Shy; F. Taroni

Heterozygous null mutation in the P₀ gene associated with mild Charcot-Marie-Tooth disease

D. Pareyson, D. Menichella, S. Botti, A. Sghirlanzoni, E. Fallica, M. Mora, C. Ciano, M. E. Shy, F. Taroni

Fondazione IRCCS Istituto Neurologico "C. Besta"

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	477-480
Number of pages	4
Journal	Annals of the New York Academy of Sciences
Volume	883
Publication status	Published - 1999

ASJC Scopus subject areas

Biochemistry, Genetics and Molecular Biology(all)

Cite this

@article{5ceb028058ff4dd7a19ff3d213dd2617,

title = "Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease",

author = "D. Pareyson and D. Menichella and S. Botti and A. Sghirlanzoni and E. Fallica and M. Mora and C. Ciano and Shy, {M. E.} and F. Taroni",

year = "1999",

language = "English",

volume = "883",

pages = "477--480",

journal = "Annals of the New York Academy of Sciences",

issn = "0077-8923",

publisher = "Wiley-Blackwell",

}

TY - JOUR

T1 - Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease

AU - Pareyson, D.

AU - Menichella, D.

AU - Botti, S.

AU - Sghirlanzoni, A.

AU - Fallica, E.

AU - Mora, M.

AU - Ciano, C.

AU - Shy, M. E.

AU - Taroni, F.

PY - 1999

Y1 - 1999

UR - http://www.scopus.com/inward/record.url?scp=0033554304&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0033554304&partnerID=8YFLogxK

M3 - Article

C2 - 10586278

AN - SCOPUS:0033554304

VL - 883

SP - 477

EP - 480

JO - Annals of the New York Academy of Sciences

JF - Annals of the New York Academy of Sciences

SN - 0077-8923

ER -

Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease

ASJC Scopus subject areas

Other files and links

Cite this

Heterozygous null mutation in the P₀ gene associated with mild Charcot-Marie-Tooth disease