论文信息 - A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans. - 字舞流文

A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.

W. Reardon | R. Winter | S. Malcolm | D. Wilkes | P. Rutland | L. Pulleyn | C. Moss | J. Ellis