The SLC26A4 c.706C>G (p.Leu236Val) Variant is a Frequent Cause of Hearing Impairment in Filipino Cochlear Implantees-Reference-Cited by-同舟云学术

The SLC26A4 c.706C>G (p.Leu236Val) Variant is a Frequent Cause of Hearing Impairment in Filipino Cochlear Implantees

Published:2018-09 Issue:8 Volume:39 Page:e726-e730
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:

Author:

Chiong Charlotte M.,Reyes-Quintos Ma. Rina T.,Yarza Talitha Karisse L.,Tobias-Grasso Celina Ann M.,Acharya Anushree,Leal Suzanne M.,Mohlke Karen L.,Mayol Nanette L.,Cutiongco-de la Paz Eva Maria,Santos-Cortez Regie Lyn P.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Sensory Systems,Otorhinolaryngology

Reference23 articles.

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3. High carrier frequency of the 35delG deafness mutation in European populations. Genetic analysis consortium of GJB2 35delG;Gasparini;Eur J Hum Genet,2000

4. Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients;Oliveira;Clin Genet,2002

5. Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East;Shahin;Hum Genet,2002

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3. Screening Strategies for Deafness Genes and Functional Outcomes in Cochlear Implant Patients;Otology & Neurotology;2021-01

4. Outcomes of Cochlear Implantation in Patients with Pendred syndrome: A Systematic Review and Narrative Synthesis;The Journal of International Advanced Otology;2020-10-19

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