Novel pathogenic variants underlie SLC26A4 -related hearing loss in a multiethnic cohort
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
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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. SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management;Genes;2022-11-23
3. Congenital hearing loss: a literature review of the genetic etiology in a Mexican population;Boletín Médico del Hospital Infantil de México;2022-09-14
4. Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNA Ala 5601C>T and tRNA Leu(CUN) 12311T>C mutations;Journal of Clinical Laboratory Analysis;2022-02-26
5. Sordera neurosensorial congénita con malformación de oído interno ligada al X en una familia mexicana;Revista de Investigación e Innovación en Ciencias de la Salud;2022-02-05
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