Literature DB >> 17536055

Mutations in VAPB are not associated with sporadic ALS.

J Kirby1, C A A Hewamadduma, J A Hartley, H C Nixon, H Evans, R R Wadhwa, C Kershaw, P G Ince, P J Shaw.   

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Year:  2007        PMID： 17536055     DOI： 10.1212/01.wnl.0000263195.50981.a6

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  4 in total

Review 1.  Clinical neurogenetics: amyotrophic lateral sclerosis.

Authors:  Matthew B Harms; Robert H Baloh
Journal:  Neurol Clin       Date:  2013-11       Impact factor: 3.806

Review 2.  VAP Proteins - From Organelle Tethers to Pathogenic Host Interactors and Their Role in Neuronal Disease.

Authors:  Suzan Kors; Joseph L Costello; Michael Schrader
Journal:  Front Cell Dev Biol       Date:  2022-06-08

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

Authors:  A D Funke; M Esser; A Krüttgen; J Weis; M Mitne-Neto; M Lazar; A L Nishimura; A D Sperfeld; P Trillenberg; J Senderek; M Krasnianski; M Zatz; S Zierz; M Deschauer
Journal:  Clin Genet       Date:  2010-03       Impact factor: 4.438

Review 4.  Flightless flies: Drosophila models of neuromuscular disease.

Authors:  Thomas E Lloyd; J Paul Taylor
Journal:  Ann N Y Acad Sci       Date:  2010-01       Impact factor: 5.691
  4 in total

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