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myopathy, reducing body, x-linked, severe early-onset
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FHL1
An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1
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