Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families-Reference-Cited by-同舟云学术

Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families

Published:2017-08 Issue: Volume:800-802 Page:29-36
ISSN:0027-5107
Container-title:Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis
language:en
Short-container-title:Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

Author:

Alkowari Moza K.,Vozzi Diego,Bhagat Shruti,Krishnamoorthy Navaneethakrishnan,Morgan Anna,Hayder Yousra,Logendra Barathy,Najjar Nehal,Gandin Ilaria,Gasparini Paolo,Badii Ramin,Girotto Giorgia,Abdulhadi Khalid

Funder

Qatar National Research Fund

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology

Reference51 articles.

1. American college of medical genetics and genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss;Alford;Genet. Med.,2014

2. Consanguinity and hereditary hearing loss in qatar;Girotto;Hum. Hered.,2014

3. Consanguinity and its relevance to clinical genetics;Bittles;Clin. Genet.,2001

4. Is there any association between consanguinity and hearing loss;Bener;Int. J. Pediatr. Otorhinolaryngol.,2005

5. GJB2 mutations and degree of hearing loss: a multicenter study;Snoeckx;Am. J. Hum. Genet.,2005

Cited by 22 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. Genetic analysis of 106 sporadic cases with hearing loss in the UAE population;Human Genomics;2024-06-07

2. Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia;Annals of Human Genetics;2024-03-22

3. The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar;Scientific Reports;2024-02-20

4. Identification of novel gene variants causing autosomal recessive non-syndromic hearing loss in Iranian families;2024-02-20

5. The natural history, clinical outcomes, and genotype–phenotype relationship of otoferlin-related hearing loss: a systematic, quantitative literature review;Human Genetics;2023-09-07