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Paper Details

Exome analysis of a family with pleiotropic congenital heart disease.
Circ Cardiovasc Genet
44
2012
Ala290Pro, CHD, CHDs, Myh6 Ala290Pro, congenital heart defects, high, indels, patient, patients, pleiotropic CHD, pleiotropic congenital heart disease, rare variants, secundum atrial septal defect, single gene defects, tricuspid atresia

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