Detection of Rare Nonsynonymous Variants in TGFB1 in Otosclerosis Patients.

Autor: Thys, M.1, Schrauwen, I.1, Vanderstraeten, K.1, Dieltjens, N.1, Fransen, E.1, Ealy, M.2, Cremers, C. W. R. J.3, van de Heyning, P.4, Vincent, R.5, Offeciers, E.6, Smith, R. H.2, van Camp, G.1 guy.vancamp@ua.ac.be
Zdroj: Annals of Human Genetics. Mar2009, Vol. 73 Issue 2, p171-175. 5p. 2 Charts.
Databáze: Academic Search Ultimate