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CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation
Abid, Fatima, Tardy, Véronique, Gaouzi, Ahmed, El hessni, Aboubaker, Morel, Yves, Chabraoui, LayachiVolume:
46
Language:
english
Journal:
Clinical Chemistry and Laboratory Medicine
DOI:
10.1515/CCLM.2008.339
Date:
January, 2008
File:
PDF, 173 KB
english, 2008