A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.
暂无分享,去创建一个
W. Reardon | R. Winter | S. Malcolm | D. Wilkes | P. Rutland | L. Pulleyn | C. Moss | J. Ellis
暂无分享,去创建一个
W. Reardon | R. Winter | S. Malcolm | D. Wilkes | P. Rutland | L. Pulleyn | C. Moss | J. Ellis