Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis

Published:2013-02-26 Issue:12 Volume:22 Page:2350-2360
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Kabashi Edor,El Oussini Hajer,Bercier Valérie,Gros-Louis François,Valdmanis Paul N.,McDearmid Jonathan,Mejier Inge A.,Dion Patrick A.,Dupre Nicolas,Hollinger David,Sinniger Jérome,Dirrig-Grosch Sylvie,Camu William,Meininger Vincent,Loeffler Jean-Philippe,René Frédérique,Drapeau Pierre,Rouleau Guy A.,Dupuis Luc

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/22/12/2350/14138920/ddt080.pdf

Reference44 articles.

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3. Genetics of familial and sporadic amyotrophic lateral sclerosis;Gros-Louis;Biochim. Biophys. Acta,2006

4. A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis;Nishimura;Am. J. Hum. Genet.,2004

5. Characterisation of the properties of a novel mutation in VAPB in familial ALS;Chen;J. Biol. Chem.,2010

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