Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population

Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population

<p>Abstract</p> <p>Recessively inherited phenotypes are frequent in the Palestinian population, as the result of a historical tradition of marriages within extended kindreds, particularly in isolated villages. In order to characterise the genetics of inherited hearing loss in this...

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Bibliographic Details
Main Authors: Walsh Tom, Rayan Amal, Sa'ed Judeh, Shahin Hashem, Shepshelovich Jeanne, Lee Ming K, Hirschberg Koret, Tekin Mustafa, Salhab Wa'el, Avraham Karen B, King Mary-Claire, Kanaan Moien
Format: Article
Language:English
Published: BMC 2006-01-01
Series:Human Genomics
Subjects:
genetics
genomics
inherited
deafness
hearing loss
mutation
Palestinian
TMPRSS3
pendrin
otoancorin
Online Access:http://www.humgenomics.com/content/2/4/203

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http://www.humgenomics.com/content/2/4/203

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