Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans-Reference-Cited by-同舟云学术

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Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans

Published:2004-11-10 Issue:1 Volume:14 Page:103-111
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Zheng Qing Yin,Yan Denise,Ouyang Xiao Mei,Du Li Lin,Yu Heping,Chang Bo,Johnson Kenneth R.,Liu Xue Zhong

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/1/103/6949064/ddi010.pdf

Reference34 articles.

1. Bolz, H., von Brederlow, B., Ramirez, A., Bryda, E.C., Kutsche, K., Nothwang, H.G., Seeliger, M., del, C.S.C.M., Vila, M.C., Molina, O.P. et al. ( 2001 ) Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome typ. 1D. Nat. Genet. , 27 , 108 –112.

2. Bork, J.M., Peters, L.M., Riazuddin, S., Bernstein, S.L., Ahmed, Z.M., Ness, S.L., Polomeno, R., Ramesh, A., Schloss, M., Srisailpathy, C.R. et al. ( 2001 ) Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23 . Am. J. Hum. Genet. , 68 , 26 –37.

3. Ahmed, Z.M., Riazuddin, S., Bernstein, S.L., Ahmed, Z., Khan, S., Griffith, A.J., Morell, R.J., Friedman, T.B. and Wilcox, E.R. ( 2001 ) Mutations of the protocadherin gene PCDH15 cause Usher syndrome typ. 1F. Am. J. Hum. Genet. , 69 , 25 –34.

4. Alagramam, K.N., Yuan, H., Kuehn, M.H., Murcia, C.L., Wayne, S., Srisailpathy, C.R., Lowry, R.B., Knaus, R., Van Laer, L., Bernier, F.P. et al. ( 2001 ) Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. Hum. Mol. Genet. , 10 , 1709 –1718.

5. Ahmed, Z.M., Riazuddin, S., Ahmad, J., Bernstein, S.L., Guo, Y., Sabar, M.F., Sieving, P., Riazuddin, S., Griffith, A.J., Friedman, T.B. et al. ( 2003 ) PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Hum. Mol. Genet. , 12 , 3215 –3223.

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