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Reply: The p.Ser107Leu in BICD2 is a mutation 'hot spot' causing distal spinal muscular atrophy. (2015)

First Author: Rossor AM

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awv160

PubMed Identifier: 26063657

Publication URI: http://europepmc.org/abstract/MED/26063657

Type: Journal Article/Review

Volume: 138

Parent Publication: Brain : a journal of neurology

Issue: Pt 11

ISSN: 0006-8950