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Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of Macedonia Cover

Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of Macedonia

Balkan Journal of Medical Genetics
Volume 13 (2010): Issue 2 (December 2010)
By:  and    
Open Access
|Jan 2011
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DOI: https://doi.org/10.2478/v10034-010-0023-7 | Journal eISSN: 2199-5761
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Language: English
Page range: 27 - 33
Published on: Jan 20, 2011
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Keywords:
Congenital adrenal hyperplasia (CAH),
21-hydroxylase deficiency,
CYP21 gene,
IVS-II-655 (C/ A>G) mutation
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2011 V Anastasovska, M Kocova, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons License.

Volume 13 (2010): Issue 2 (December 2010)