Population Data on D7S2425 Marker in Five Ethnic Groups of the Iranian Population: A Highly Informative Marker for Molecular Diagnosis of ARNSHL

Background & Aims: SLC26A4 gene mutations are the second identifiable genetic cause of autosomal recessive nonsyndromic hearing loss (ARNSHL) after GJB2 mutations and are currently investigated in molecular diagnosis.In databases, several potential STR markers related to this region have been introd...

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Autori principali:	Marjan Mojtabavi Naeini, Sadeq Vallian Boroujeni, Morteza Hashemzadeh Chaleshtori
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Kerman University of Medical Sciences 2014-01-01
Serie:	Journal of Kerman University of Medical Sciences
Soggetti:	d7s2425 marker slc26a4 autosomal recessive nonsyndromic hearing loss (arnshl) iranian population
Accesso online:	https://jkmu.kmu.ac.ir/article_16146_fa6dea2eff656374c096a8741a0d4318.pdf
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