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myopathy, x-linked
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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
The developmental regulation of a novel muscle LIM-protein
MTM1
Genomic organization of the MTM1 gene implicated in X-linked myotubular myopathy.
Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1).
Cancer Gene Census
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Inositol phosphate metabolism
Homo sapiens (human)
one gene
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External
Molecular and Genetic Studies of Congenital Myopathies