Emerging complexities of the mouse as a model for human hearing loss-Reference-Cited by-同舟云学术

Emerging complexities of the mouse as a model for human hearing loss

Published:2022-08-12 Issue:35 Volume:119 Page:
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proc. Natl. Acad. Sci. U.S.A.

Author:

Carlson Ryan J.¹²^ORCID,Avraham Karen B.³^ORCID

Affiliation:

1. Department of Genome Sciences, University of Washington, Seattle, WA 98195

2. Department of Medicine, University of Washington, Seattle, WA 98195

3. Department of Human Molecular Genetics and Biochemistry, Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, Tel Aviv 6997801, Israel

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Link

https://pnas.org/doi/pdf/10.1073/pnas.2211351119

Reference25 articles.

1. Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice

2. Mouse screen reveals multiple new genes underlying mouse and human hearing loss

3. Loss of MINAR2 impairs motor function and causes Parkinson’s disease-like symptoms in mice

4. Shaker, a New Mutation of the House Mouse (Mus musculus)

5. Mouse ENU Mutagenesis

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