A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family-Reference-Cited by-同舟云学术

A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family

Published:2016-08 Issue: Volume:87 Page:28-33
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Behlouli Asma,Bonnet Crystel,Abdi Samia,Hasbellaoui Mokhtar,Boudjenah Farid,Hardelin Jean-Pierre,Louha Malek,Makrelouf Mohamed,Ammar-Khodja Fatima,Zenati Akila,Petit Christine

Funder

LHW-Stiftung, European Research Council

Foundation BNP Paribas

Algerian government

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference50 articles.

1. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population;Marazita;AmJ Med. Genet.,1993

2. Genetic epidemiology of hearing impairment;Morton;Ann. N. Y. Acad. Sci.,1991

3. Sensorineural hearing loss in children;Smith;Lancet,2005

4. Nonsyndromic Hearing Loss and Deafness;Smith,1993

5. Current concepts: newborn hearing screening - a silent revolution;Morton;New Engl. J. Med.,2006

Cited by 11 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. Custom Next‐Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys;Molecular Genetics & Genomic Medicine;2022-01-08

2. Hearing loss in Africa: current genetic profile;Human Genetics;2021-10-05

3. Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families;Neural Plasticity;2021-04-22

4. Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next‐generation sequencing;Journal of Clinical Laboratory Analysis;2020-08-30

5. Genetic Epidemiology of Hearing Loss in the 22 Arab Countries: A Systematic Review;Otology & Neurotology;2020-02