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Literature DB >> 9354784

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.

X Z Liu, J Walsh, Y Tamagawa, K Kitamura, M Nishizawa, K P Steel, S D Brown.

Abstract

Entities: Disease Gene Mutation

Mesh：

Substances：
Myosins

Year: 1997 PMID： 9354784 DOI： 10.1038/ng1197-268

Source DB: PubMed Journal: Nat Genet ISSN： 1061-4036 Impact factor: 38.330

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80 in total

1. Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion.

Authors: M C Lanasa; W A Hogge; C Kubik; J Blancato; E P Hoffman
Journal: Am J Hum Genet Date: 1999-07 Impact factor: 11.025

2. A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

Authors: K Fukushima; N Kasai; Y Ueki; K Nishizaki; K Sugata; S Hirakawa; A Masuda; M Gunduz; Y Ninomiya; Y Masuda; M Sato; W T McGuirt; P Coucke; G Van Camp; R J Smith
Journal: Am J Hum Genet Date: 1999-07 Impact factor: 11.025

3. Inherited deafness in childhood--the genetic revolution unmasks the clinical challenge.

Authors: W Reardon; R F Mueller
Journal: Arch Dis Child Date: 2000-04 Impact factor: 3.791

Review 4. Towards a molecular understanding of Drosophila hearing.

Authors: Jason C Caldwell; Daniel F Eberl
Journal: J Neurobiol Date: 2002-11-05

5. 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

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.

1. Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion.

2. A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

3. Inherited deafness in childhood--the genetic revolution unmasks the clinical challenge.

Review 4. Towards a molecular understanding of Drosophila hearing.

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

Review 6. Anatomical and molecular design of the Drosophila antenna as a flagellar auditory organ.

Review 7. Genetics and pathological mechanisms of Usher syndrome.

8. Myosin VI and VIIa distribution among inner ear epithelia in diverse fishes.

Review 9. Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

10. A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.