Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
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Characterising the spectrum of autosomal recessive hereditary hearing loss in IranComprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohortMicroRNAs in inner ear biology and pathogenesis.The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations.The promise of whole-exome sequencing in medical genetics.Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families.Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP GeneMutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran.An overview of mutation detection methods in genetic disorders.Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian families.Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran.GJB2 mutations in deaf population of Ilam (Western Iran): a different pattern of mutation distribution.Clinical Application of Screening for GJB2 Mutations before Cochlear Implantation in a Heterogeneous Population with High Rate of Autosomal Recessive Nonsyndromic Hearing Loss.GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population.Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations.GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family.
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Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 26 August 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
@en
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
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type
label
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
@en
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
@nl
prefLabel
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
@en
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
@nl
P2093
P2860
P356
P1476
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
@en
P2093
Bahareh Rabbani
Mohammad Taghi Akbari
Nejat Mahdieh
Sirous Zeinali
Susan Wiley
P2860
P2888
P304
P356
10.1038/JHG.2010.96
P577
2010-08-26T00:00:00Z