论文信息 - Combined 17α-hydroxylase/17,20-lyase deficiency due to p.R96W mutation in the CYP17 gene in a Brazilian patient. - 字舞流文

Combined 17α-hydroxylase/17,20-lyase deficiency due to p.R96W mutation in the CYP17 gene in a Brazilian patient.

R. Auchus | T. C. Rodrigues | C. Kater | M. Czepielewski | M. Papari-Zareei | Fabíola Costenaro