Genetic hearing loss: the journey of discovery to destination – how close are we to therapy?-Reference-Cited by-同舟云学术

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Genetic hearing loss: the journey of discovery to destination – how close are we to therapy?

Published:2016-11 Issue:6 Volume:4 Page:583-587
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Pandya Arti¹

Affiliation:

1. Division of Genetics and Metabolism Department of Pediatrics University of North Carolina Chapel Hill North Carolina

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.260

Reference40 articles.

1. Restoration of Hearing in the VGLUT3 Knockout Mouse Using Virally Mediated Gene Therapy

2. Tmc gene therapy restores auditory function in deaf mice

3. Whole-exome sequencing and its impact in hereditary hearing loss

4. Azaiez H. G.Van Camp andR. J.Smith.2006.Connexins and deafness: from molecules to disease.27:148–159.

5. EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness

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1. Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review;Biomedicines;2023-06-12

2. Genetic etiology of hearing loss in Iran;Human Genetics;2022-01-20

3. Racial and ethnic disparities in genetic testing for hearing loss: a systematic review and synthesis;Human Genetics;2021-09-07

4. Genetic Determinants of Non-Syndromic Enlarged Vestibular Aqueduct: A Review;Audiology Research;2021-08-28

5. Auditory Neuropathy Spectrum Disorder (ANSD)—Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families;BioMed Research International;2020-12-22

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