Heterozygous mutation ofUsh1g/Sansin mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation inCdh23

Author:

Miyasaka Yuki,Shitara Hiroshi,Suzuki Sari,Yoshimoto Sachi,Seki Yuta,Ohshiba Yasuhiro,Okumura Kazuhiro,Taya Choji,Tokano Hisashi,Kitamura Ken,Takada Toyoyuki,Hibino Hiroshi,Shiroishi Toshihiko,Kominami Ryo,Yonekawa Hiromichi,Kikkawa Yoshiaki

Funder

Japan Society for the Promotion of Science KAKENHI

JSPS

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference65 articles.

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2. Genetics and pathological mechanisms of Usher syndrome

3. Genetic Mapping and Exome Sequencing Identify Variants Associated with Five Novel Diseases

4. The Mechanosensory Structure of the Hair Cell Requires Clarin-1, a Protein Encoded by Usher Syndrome III Causative Gene

5. Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction

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