Functional and Structural Study of the Amino Acid Substitution in a Novel Familial Androgen Receptor Mutation (W752G) Responsible for Complete Androgen Insensitivity Syndrome
pubblicato in: Sexual Development
data di pubblicazione: 2018-08-01
argomento principale: complete androgen insensitivity syndrome
Cita articoli
There is nothing here
Articolo - wd:Q90665979