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H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations? (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/10.1002/mds.26129

PubMed Identifier: 25545912

Publication URI: http://europepmc.org/abstract/MED/25545912

Type: Journal Article/Review

Volume: 30

Parent Publication: Movement disorders : official journal of the Movement Disorder Society

Issue: 6

ISSN: 0885-3185