This clinical condition, which is extremely rare, is very interesting for researchers involved in studies regarding sex determination processes, because the molecular analysis of such patients could lead to the discovery of genes involved in testis differentiation in the absence of the master gene SRY. Unfortunately, the article includes a number of inaccuracies and omissions regarding the state of the art on clinical features and genetic studies of this condition in human patients and animal models. Consequently some aspects of it ought to be revised or clarified.
PARMA, PIETRO (Primo)
|Settore Scientifico Disciplinare:||Settore BIO/13 - Biologia Applicata|
|Data di pubblicazione:||2010|
|Appare nelle tipologie:||01 - Articolo su periodico|