A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct-Reference-Cited by-同舟云学术

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A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct

Published:2018-04 Issue: Volume:107 Page:97-100
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Liang Yuan,Peng Qi,Wang Kangwei,Zhu Pengyuan,Wu Chunqiu,Rao Chunbao,Chang Jiang,Li Siping,Lu Xiaomei^ORCID

Funder

Dongguan Bureau of Science and Technology for the City Key Program of Science and Technology

Science and Technology Planning Project of Guangdong Province

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference28 articles.

1. Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss;Okamoto;Laryngoscope,2014

2. Newborn hearing screening–a silent revolution;Morton;N. Engl. J. Med.,2006

3. Audiometric findings in children with a large vestibular aqueduct;Arjmand;Arch. Otolaryngol. Head Neck Surg.,2004

4. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (pds);Everett;Nat. Genet.,1997

5. Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?;Hilgert;Mutat. Res.,2009

Cited by 2 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. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options;Clinical Genetics;2022-09-29

2. Ulinastatin Reduces the Severity of Intestinal Damage in the Neonatal Rat Model of Necrotizing Enterocolitis;Medical Science Monitor;2019-12-01

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