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Homozygous complete deletion of CYP21A2 causes a simple virilizing phenotype in an Azeri child Cover

Homozygous complete deletion of CYP21A2 causes a simple virilizing phenotype in an Azeri child

Asian Biomedicine
Volume 5 (2011): Issue 6 (December 2011)
By: Bahareh Rabbani,  Mohammad Taghi Akbari,  Nejat Mahdieh,  Ehya Zaridust,  Mohammad Taghi Haghi Ashtiani,  Hsien-Hsiung Lee,  Richard Auchus and  Ali Rabbani  
Open Access
|Feb 2017
DOI: https://doi.org/10.5372/1905-7415.0505.042 | Journal eISSN: 1875-855X | Journal ISSN: 1905-7415
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Language: English
Page range: 889 - 892
Published on: Feb 4, 2017
Published by: Chulalongkorn University
In partnership with: Paradigm Publishing Services
Publication frequency: 6 issues per year
Keywords:
Azeri family,
congenital adrenal hyperplasia,
simple virilizing
Related subjects:
Medicine,
Assistive professions, nursing,
Basic medical science,
Basic medical science, other,
Clinical medicine,
Clinical medicine, other

© 2017 Bahareh Rabbani, Mohammad Taghi Akbari, Nejat Mahdieh, Ehya Zaridust, Mohammad Taghi Haghi Ashtiani, Hsien-Hsiung Lee, Richard Auchus, Ali Rabbani, published by Chulalongkorn University
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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