Genotype–phenotype correlations for SLC26A4-related deafness-Reference-Cited by-同舟云学术

Genotype–phenotype correlations for SLC26A4-related deafness

Published:2007-08-10 Issue:5 Volume:122 Page:451-457
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Azaiez Hela,Yang Tao,Prasad Sai,Sorensen Jessica L.,Nishimura Carla J.,Kimberling William J.,Smith Richard J. H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-007-0415-2.pdf

Reference34 articles.

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2. Albert S, Blons H, Jonard L, Feldmann D, Chauvin P, Loundon N, Sergent-Allaoui A, Houang M, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Dollfus H, Eliot MM, David A, Calais C, Drouin-Garraud V, Obstoy MF, Tran Ba Huy P, Lacombe D, Duriez F, Francannet C, Bitoun P, Petit C, Garabedian EN, Couderc R, Marlin S, Denoyelle F (2006) SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations. Eur J Hum Genet 14:773–779

3. Azaiez H, Smith R (2007) Temporal bone imaging in GJB2 Deafness. Laryngoscope 117(6):1127

4. Ballana E, Ventayol M, Rabionet R, Gasparini P, Estivill X (2007) Connexins and deafness Homepage. World wide web URL: http://www.davinci.crg.es/deafness/

5. Campbell C, Cucci RA, Prasad S, Green GE, Edeal JB, Galer CE, Karniski LP, Sheffield VC, Smith RJ (2001) Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype–phenotype correlations. Hum Mutat 17:403–411

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