A Novel Mutation in a Kazakh Family with X-Linked Alport Syndrome

Open Access

Peer-reviewed

Research Article

Barshagul T. Baikara ,

Contributed equally to this work with: Barshagul T. Baikara, Elena V. Zholdybayeva

* E-mail: baikara.barshagul@gmail.com

Affiliation National Center for Biotechnology, Astana, Kazakhstan
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Elena V. Zholdybayeva ,

Contributed equally to this work with: Barshagul T. Baikara, Elena V. Zholdybayeva

Affiliation National Center for Biotechnology, Astana, Kazakhstan
⨯
Saule E. Rakhimova,

Affiliations National Center for Biotechnology, Astana, Kazakhstan, Center for Sciences, Nazarbayev University, Astana, Kazakhstan
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Nazym B. Nigmatullina,

Affiliation National Research Center for Maternal and Child Health, Astana, Kazakhstan
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Kuvat T. Momynaliev,

Affiliation National Center for Biotechnology, Astana, Kazakhstan
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Yerlan M. Ramanculov

Affiliations National Center for Biotechnology, Astana, Kazakhstan, School of Science and Technology, Nazarbayev University, Astana, Kazakhstan
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X-linked traits
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Collagens
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Mutation detection
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Chronic kidney disease
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Deafness
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Glycine
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Kazakh people
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Renal failure
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