Nonsyndromic Hearing Loss Caused by USH1G Mutations-Reference-Cited by-同舟云学术

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Nonsyndromic Hearing Loss Caused by USH1G Mutations

Published:2015-03 Issue:2 Volume:36 Page:205-211
ISSN:0196-0202
Container-title:Ear & Hearing
language:en
Short-container-title:

Author:

Maria Oonk Anne Marthe,van Huet Ramon A. C.,Leijendeckers Joop M.,Oostrik Jaap,Venselaar Hanka,van Wijk Erwin,Beynon Andy,Kunst Henricus P. M.,Hoyng Carel B.,Kremer Hannie,Schraders Margit,Pennings Ronald J. E.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Speech and Hearing,Otorhinolaryngology

Reference1 articles.

1. M. R., Bosman A. J., Huygen P. L. M., et al. ). Audiological characteristics of some affected members of a dutch DFNA13 COL11A2 family.;De Leenheer;Ann Otol Rhinol Laryngol,2004

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1. Combined Presence in Heterozygosis of Two Variant Usher Syndrome Genes in Two Siblings Affected by Isolated Profound Age-Related Hearing Loss;Biomedicines;2023-09-28

2. The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification;Human Genetics;2022-03-30

3. Usher Syndrome: Genetics of a Human Ciliopathy;International Journal of Molecular Sciences;2021-06-23

4. Usher Syndrome: Genetics and Molecular Links of Hearing Loss and Directions for Therapy;Frontiers in Genetics;2020-10-22

5. Usher syndrome: diagnostic approach, differential diagnoses and proposal of an updated function-based genetic classification;Medizinische Genetik;2020-08-01

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