A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations

Published 2010 View Full Article

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Title
A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations
Authors
Keywords
-
Journal
JOURNAL OF THE NEUROLOGICAL SCIENCES
Volume 296, Issue 1-2, Pages 22-29
Publisher
Elsevier BV
Online
2010-07-15
DOI
10.1016/j.jns.2010.06.017

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