Only two mutations detected in 15 Tunisian patients with 11β‐hydroxylase deficiency: the p.Q356X and the novel p.G379V
暂无分享,去创建一个
L. B. Jemaa | Y. Morel | S. Barsaoui | H. Chaabouni | M. Kharrat | L. Kraoua | M. Châabouni | F. Maazoul | L. Ben Jemaa | N. Gandoura | S. Trabelsi | R. M'rad | L. Ben Jemâa