Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.

Wang, Binbin

Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect. [electronic resource] - International journal of cardiology Nov 2010 - 83-5 p. digital

Publication Type: Comparative Study; Letter; Research Support, Non-U.S. Gov't

1874-1754

10.1016/j.ijcard.2009.05.030 doi


Amino Acid Sequence
Asian People--genetics
Cohort Studies
Forkhead Transcription Factors--genetics
Genetic Variation--genetics
Heart Septal Defects, Ventricular--diagnosis
Humans
Molecular Sequence Data
Mutation--genetics