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

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

Balkan Journal of Medical Genetics
Volume 13 (2010): Issue 1 (June 2010)
By: V Anastasovska,  E Kocova and  M Kocova  
Open Access
|Aug 2010
DOI: https://doi.org/10.2478/v10034-010-0014-8 | Journal eISSN: 2199-5761
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Language: English
Page range: 17 - 21
Published on: Aug 25, 2010
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
CYP21A2 gene,
21-Hydroxylase deficiency,
Nonclassical congenital adrenal hyperplasia (NCAH),
p.P30L Mutation
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2010 V Anastasovska, E Kocova, M Kocova, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons License.

Volume 13 (2010): Issue 1 (June 2010)