Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D-Reference-Cited by-同舟云学术

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

Published:2001-01 Issue:1 Volume:27 Page:108-112
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Bolz Hanno,von Brederlow Benigna,Ramírez Alfredo,Bryda Elizabeth C.,Kutsche Kerstin,Nothwang Hans Gerd,Seeliger Mathias,Cabrera Maria del C.-Salcedó,Vila Manuel Caballeró,Molina Orfilio Pelaez,Gal Andreas,Kubisch Christian

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0101_108.pdf

Reference27 articles.

1. Keats, B.J. & Corey, D.P. The usher syndromes. Am. J. Med. Genet. 89, 158–166 (1999).

2. Weil, D. et al. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 374, 60–61 (1995).

3. Verpy, E. et al. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies usher syndrome type 1C. Nature Genet. 26, 51–55 (2000).

4. Bitner-Glindzicz, M. et al. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the usher type 1C gene. Nature Genet. 26, 56–60 ( 2000).

5. Wayne, S. et al. Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10. Hum. Mol. Genet. 5, 1689– 1692 (1996).

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