Using Drosophila to study mechanisms of hereditary hearing loss.

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Using Drosophila to study mechanisms of hereditary hearing loss.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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Using Drosophila to study mechanisms of hereditary hearing loss.

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Using Drosophila to study mechanisms of hereditary hearing loss.

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Using Drosophila to study mechanisms of hereditary hearing loss.

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Using Drosophila to study mechanisms of hereditary hearing loss.

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Using Drosophila to study mechanisms of hereditary hearing loss.

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Using Drosophila to study mechanisms of hereditary hearing loss.

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P1476

Using Drosophila to study mechanisms of hereditary hearing loss.

@en

P2093

Tongchao Li

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P275

Creative Commons Attribution

P2860

Drosophila TRPN(=NOMPC) channel localizes to the distal end of mechanosensory cilia

Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype

Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment

Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3.

Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9

Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa

Homophila: human disease gene cognates in Drosophila

P31

scholarly article

review article

P356

10.1242/DMM.031492

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P433

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P478

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P50

Hugo J. Bellen

Andrew K. Groves

P5008

ScienceSource

P577

2018-05-31T00:00:00Z

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P698

29853544

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P921

Chin-hu̍t seng-bu̍t

sensorineural hearing loss

P932

6031363

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