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A novel TUBB4A mutation suggests that genotype-phenotype correlation of H-ABC syndrome needs to be revisited. (2015)

First Author: Erro R

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/awu403

PubMed Identifier: 25614026

Publication URI: http://europepmc.org/abstract/MED/25614026

Type: Journal Article/Review

Volume: 138

Parent Publication: Brain : a journal of neurology

Issue: Pt 8

ISSN: 0006-8950