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Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations
Concolino, Paola, Mello, Enrica, Zuppi, Cecilia, Capoluongo, EttoreVolume:
48
Language:
english
Journal:
Clinical Chemistry and Laboratory Medicine
DOI:
10.1515/CCLM.2010.239
Date:
January, 2010
File:
PDF, 136 KB
english, 2010