A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia

A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia

Bibliographic Details
Main Authors:	Anastasovska V, Kocova E, Kocova M
Format:	Article
Language:	English
Published:	Sciendo 2010-01-01
Series:	Balkan Journal of Medical Genetics
Subjects:	cyp21a2 gene 21-hydroxylase deficiency nonclassical congenital adrenal hyperplasia (ncah) p.p30l mutation
Online Access:	https://doi.org/10.2478/v10034-010-0014-8

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