CYP21A2 p.E238 deletion as result of multiple microconversion events: a genetic study on an Italian congenital adrenal hyperplasia (CAH) family / Concolino, P; Mello, E; Zuppi, C; Toscano, V; Capoluongo, E.. - In: DIAGNOSTIC MOLECULAR PATHOLOGY. - ISSN 1052-9551. - 22:(2013), pp. 48-51.

CYP21A2 p.E238 deletion as result of multiple microconversion events: a genetic study on an Italian congenital adrenal hyperplasia (CAH) family

Capoluongo E.
2013

2013
CYP21A2 p.E238 deletion as result of multiple microconversion events: a genetic study on an Italian congenital adrenal hyperplasia (CAH) family / Concolino, P; Mello, E; Zuppi, C; Toscano, V; Capoluongo, E.. - In: DIAGNOSTIC MOLECULAR PATHOLOGY. - ISSN 1052-9551. - 22:(2013), pp. 48-51.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/780110
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