Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patients.

Thys, M

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