Mutations in the PDS Gene in German Families with Pendred’s Syndrome: V138F Is a Founder Mutation-Reference-Cited by-同舟云学术

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Mutations in the PDS Gene in German Families with Pendred’s Syndrome: V138F Is a Founder Mutation

Published:2003-06 Issue:6 Volume:88 Page:2916-2921
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Borck Guntram,Roth Christian,Martiné Ursula,Wildhardt Gabriele,Pohlenz Joachim

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 31 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Insight into the Natural History of Pathogenic Variant c.919-2A>G in the SLC26A4 Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia (Russia);Genes;2023-04-17

2. Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss;International Journal of Molecular Sciences;2022-11-03

3. Molekulare und funktionale Abklärung hereditärer Schwerhörigkeiten am Beispiel des SLC26A4-Gens;Laryngo-Rhino-Otologie;2020-12

4. Non-syndromic hearing loss: clinical and diagnostic challenges;Medizinische Genetik;2020-08-01

5. Novel pathogenic variants underlie SLC26A4 -related hearing loss in a multiethnic cohort;International Journal of Pediatric Otorhinolaryngology;2017-10

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