The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case

The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case

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Bibliographic Details
Published in:Clinical genetics Vol. 77; no. 3; pp. 302 - 303
Main Authors: Funke, AD, Esser, M, Krüttgen, A, Weis, J, Mitne-Neto, M, Lazar, M, Nishimura, AL, Sperfeld, AD, Trillenberg, P, Senderek, J, Krasnianski, M, Zatz, M, Zierz, S, Deschauer, M
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-03-2010
Subjects:
Female
Humans
Letters to the Editor
Male
Muscle Weakness - genetics
Pedigree
Point Mutation
Vesicular Transport Proteins - genetics
Online Access:Get full text
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Description
Bibliography:ark:/67375/WNG-7TJD8F82-7
ArticleID:CGE1319
istex:54388C4DEC6B38FD2E5756CDB01E03E70A3D5F08
Both authors contributed equally.
Re‐use of this article is permitted in accordance with the Terms and Conditions set out at
http://www3.interscience.wiley.com/authorresources/onlineopen.html
Current address: Institute of Psychiatry, Kings College London, MRC Centre for Neurodegenerative Research, London, UK
ObjectType-Article-1
SourceType-Scholarly Journals-1
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Re-use of this article is permitted in accordance with the Terms and Conditions set out at http://www3.interscience.wiley.com/authorresources/onlineopen.html
ISSN:0009-9163
1399-0004
DOI:10.1111/j.1399-0004.2009.01319.x