Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness-Reference-Cited by-同舟云学术

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Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

Published:2003-04-01 Issue:4 Volume:40 Page:242-248
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:
Short-container-title:

Author:

Park H-J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 274 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. Low Efficiency of Homology-Independent Targeted Integration for CRISPR/Cas9 Correction in the Vicinity of SLC26A4 c.919–2A>G Variant;2024-06-20

2. Unraveling the Genetic Basis of Combined Deafness and Male Infertility Phenotypes through High‐Throughput Sequencing in a Unique Cohort from South India;Advanced Genetics;2024-05-08

3. The molecular principles underlying diverse functions of the SLC26 family of proteins;Journal of Biological Chemistry;2024-05

4. Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades;Journal of Cellular and Molecular Medicine;2024-03-27

5. Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia;Annals of Human Genetics;2024-03-22

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