Next‐generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss-Reference-Cited by-同舟云学术

Next‐generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss

Published:2020-10-23 Issue:12 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol. Genet. Genomic Med.

Author:

Xiang Yan‐Bao¹,Xu Chen‐Yang¹,Xu Yun‐Zhi¹,Li Huan‐Zheng¹^ORCID,Zhou Li‐Li¹,Xu Xue‐Qin¹,Chen Zi‐Hui²,Tang Shao‐Hua¹²^ORCID

Affiliation:

1. Key Laboratory of Birth Defects Department of Genetics Wenzhou Central Hospital Wenzhou China

2. Key laboratory of Medical Genetic School of Laboratory Medicine and Life Science Wenzhou Medical University Wenzhou China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1539

Reference37 articles.

1. Auditory hair cell defects as potential cause for sensorineural deafness in Wolf‐Hirschhorn syndrome;Ahmed M.;Disease Model & Mechanisms,2015

2. Identification of novel variants in MYO15A , OTOF , and RDX with hearing loss by next‐generation sequencing

3. TBC1D24genotype–phenotype correlation

4. Wolf-Hirschhorn syndrome: A review and update

5. Experience of targeted Usher exome sequencing as a clinical test

Cited by 13 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. Identification of novel and known genetic variants associated with hereditary hearing loss in iranian families using whole exome sequencing;Molecular Biology Reports;2024-05-20

2. Ursids evolved dietary diversity without major alterations in metabolic rates;Scientific Reports;2024-02-27

3. Investigation of a novel TBC1D24 variation causing autosomal dominant non-syndromic hearing loss;Scientific Reports;2024-02-27

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

5. Next‐generation sequencing for genetic testing of hearing loss populations;Clinica Chimica Acta;2024-01