Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patients. [electronic resource]
- Annals of human genetics Mar 2009
- 171-5 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1469-1809
10.1111/j.1469-1809.2009.00505.x doi
Case-Control Studies DNA Mutational Analysis Europe Female Genetic Predisposition to Disease Humans Male Mutation, Missense Otosclerosis--genetics Transforming Growth Factor beta1--genetics