Literature DB >> 9915977

A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration.

A K Lalwani, W M Luxford, A N Mhatre, A Attaie, E R Wilcox, C M Castelein.   

Abstract

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Year:  1999        PMID： 9915977      PMCID： PMC1377736          DOI： 10.1086/302216

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  6 in total

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

Authors:  A K Lalwani; J A Goldstein; M J Kelley; W Luxford; C M Castelein; A N Mhatre
Journal:  Am J Hum Genet       Date:  2000-10-09       Impact factor: 11.025

2.  Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.

Authors:  J M Bork; L M Peters; S Riazuddin; S L Bernstein; Z M Ahmed; S L Ness; R Polomeno; A Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Z Ahmed; S N Khan; V M Kaloustian; X C Li; A Lalwani; S Riazuddin; M Bitner-Glindzicz; W E Nance; X Z Liu; G Wistow; R J Smith; A J Griffith; E R Wilcox; T B Friedman; R J Morell
Journal:  Am J Hum Genet       Date:  2000-11-21       Impact factor: 11.025

3.  [Hereditary sensorineural hearing impairment and macrothrombocytopenia: a rare MYH9 gene mutation].

Authors:  A Böttcher; R Knecht; C-J Busch; B B Lörincz; C V Dalchow
Journal:  HNO       Date:  2013-02       Impact factor: 1.284

4.  Localization in stereocilia, plasma membrane, and mitochondria suggests diverse roles for NMHC-IIa within cochlear hair cells.

Authors:  Anil K Lalwani; Graham Atkin; Yan Li; Jennifer Y Lee; Dean E Hillman; Anand N Mhatre
Journal:  Brain Res       Date:  2008-01-03       Impact factor: 3.252

5.  c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.

Authors:  Vitor G L Dantas; Karina Lezirovitz; Guilherme L Yamamoto; Carolina Fischinger Moura de Souza; Simone Gomes Ferreira; Regina C Mingroni-Netto
Journal:  Genet Mol Biol       Date:  2014-11-14       Impact factor: 1.771

Review 6.  Rho-Family Small GTPases: From Highly Polarized Sensory Neurons to Cancer Cells.

Authors:  Takehiko Ueyama
Journal:  Cells       Date:  2019-01-28       Impact factor: 6.600
  6 in total

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