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Journal of the Neurological Sciences
Volume 296, Issue 1
, Pages 22-29
, 15 September 2010
A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations
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PII: S0022-510X(10)00287-X
doi: 10.1016/j.jns.2010.06.017
« Previous
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Journal of the Neurological Sciences
Volume 296, Issue 1
, Pages 22-29
, 15 September 2010
