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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease myopathy
Comorbidity C0699743|congenital muscular dystrophy
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PubMedID- 22918531 Inhibition of tgfbeta signaling by losartan treatment greatly improved the phenotype of myopathies associated with laminin-alpha2-deficient congenital muscular dystrophy.

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