Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates-Reference-Cited by-同舟云学术

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Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates

Published:2000-06 Issue:6 Volume:57 Page:439-443
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Ben Arab Saïda,Hmani Mounira,Denoyelle Françoise,Boulila-Elgaied Amel,Chardenoux Sebastien,Hachicha Slah,Petit Christine,Ayadi Hammadi

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2000.570607.x/fullpdf

Reference11 articles.

1. An epidemiological and genetic study of congenital profound deafness in Tunisia (governorate of Nabeul);Ben Arab;J Med Genet,1990

2. A non-syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q;Guilford;Nat Genet,1994

3. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness;Kelsell;Nature,1997

4. A comprehensive genetic map of the human genome based on 5.264 microsatellites;Dib;Nature,1996

5. The detection of linkage in human genetics;Smith;JR Statist Soc,1953

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4. EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness;Orphanet Journal of Rare Diseases;2014-04-17

5. Specific Aspects of Consanguinity: Some Examples from the Tunisian Population;Human Heredity;2014

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