Código QR (código de barras bidimensional)

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...

ver descrição completa

Na minha lista:
Principais autores: Marjan Mojtabavi Naeini, Sadeq Vallian Boroujeni, Morteza Hashemzadeh Chaleshtori
Formato: Artigo
Idioma:Inglês
Publicado em: Kerman University of Medical Sciences 2014-01-01
coleção:Journal of Kerman University of Medical Sciences
Assuntos:
d7s2425 marker
slc26a4
autosomal recessive nonsyndromic hearing loss (arnshl)
iranian population
Acesso em linha:https://jkmu.kmu.ac.ir/article_16146_fa6dea2eff656374c096a8741a0d4318.pdf
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registros relacionados