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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

Authors

Bahareh Rabbani

Iran (Islamic Republic of)

Mohammad Taghi Akbari

baharehrabbani@yahoo.com

Iran (Islamic Republic of)

Nejat Mahdieh

Iran (Islamic Republic of)
Iran (Islamic Republic of)

Ehya Zaridust

Iran (Islamic Republic of)
Iran (Islamic Republic of)

Mohammad Taghi Haghi Ashtiani

Iran (Islamic Republic of)
Iran (Islamic Republic of)

Hsien-Hsiung Lee

Richard Auchus

United States of America

Ali Rabbani

Iran (Islamic Republic of)
Iran (Islamic Republic of)
Iran (Islamic Republic of)
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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