Two novel mutations of the IRX4 gene in patients with congenital heart disease. [electronic resource]
- Human genetics Nov 2011
- 657-62 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1432-1203
10.1007/s00439-011-0996-7 doi
Amino Acid Sequence Asian People--genetics Base Sequence Child Cohort Studies Heart Defects, Congenital--genetics Homeodomain Proteins--genetics Humans Infant Male Molecular Sequence Data Mutation Retinoid X Receptors--metabolism