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

Internet

https://doi.org/10.2478/v10034-010-0014-8

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