Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18-Reference-Cited by-同舟云学术

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Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18

Published:1999-05-01 Issue:5 Volume:10 Page:520-522
ISSN:0938-8990
Container-title:Mammalian Genome
language:
Short-container-title:Mammalian Genome

Author:

Cohen-Salmon Martine,Mattei Marie-Geneviève,Petit Christine

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://link.springer.com/content/pdf/10.1007/s003359901033.pdf

Cited by 15 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. Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea;Scientific Reports;2020-10-22

2. Inner Ear Proteins as Potential Biomarkers;Otology & Neurotology;2020-02

3. Clinical characteristics with long-term follow-up of four Okinawan families with moderate hearing loss caused by an OTOG variant;Human Genome Variation;2019-08-13

4. The OTOGL p.Arg925* Variant is Associated with Moderate Hearing Loss in a Syrian Nonconsanguineous Family;Genetic Testing and Molecular Biomarkers;2017-07

5. A reverse genetic approach identifies an ancestral frameshift mutation in RP1 causing recessive progressive retinal degeneration in European cattle breeds;Genetics Selection Evolution;2016-08-10

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