Results 131 to 140 of about 6,492 (168)

A novel truncating variant in <i>PRDM16</i> causes severe familial cardiomyopathy with variable clinical presentations. [PDF]

open access: yesGenes Dis
Che Y   +9 more
europepmc   +1 more source

PRDM16 regulates smooth muscle cell identity and atherosclerotic plaque composition. [PDF]

open access: yesNat Cardiovasc Res
Tan JME   +15 more
europepmc   +1 more source

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