ListarFHEFD - Artículos por tema "Fenotipo"
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Fhl1 W122S causes loss of protein function and late-onset mild myopathy.
(Oxford Academic, 2014-09-30)A member of the four-and-a-half-LIM (FHL) domain protein family, FHL1, is highly expressed in human adult skeletal and cardiac muscle. Mutations in FHL1 have been associated with diverse X-linked muscle diseases: scapuloperoneal ...