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Article

A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle

21 Feb 2018

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 29468350
DOI: 10.1007/s00246-018-1822-y

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A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right VentriclePMID 29468350Read ↗

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