A systematic review and meta-analysis of common mutations of SLC26A4 gene in Asian populations
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
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3. Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PD S mutations;Usami;Hum. Genet.,1999
4. Pendred syndrome and DFNB4 -mutation screening of SLC26A 4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutations;Prasad;Am. J. Med. Genet. A,2004
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1. Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China;BMC Medical Genomics;2024-02-20
2. Carrier frequencies, trends, and geographical distribution of hearing loss variants in China: The pooled analysis of 2,161,984 newborns;Heliyon;2024-02
3. The correlation between deafness progression and SLC26A4 mutations in enlarged vestibular aqueduct patients;European Archives of Oto-Rhino-Laryngology;2023-07-21
4. 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
5. Alternative splicing in shaping the molecular landscape of the cochlea;Frontiers in Cell and Developmental Biology;2023-03-02
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