(Q37782545)

23 August 2017

title

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations (English)

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23 August 2017

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Nejat Mahdieh

1

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23 August 2017

Bahareh Rabbani

2

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23 August 2017

Susan Wiley

3

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23 August 2017

Mohammad Taghi Akbari

4

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23 August 2017

Sirous Zeinali

5

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23 August 2017

publication date

26 August 2010

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Journal of Human Genetics

23 August 2017

published in

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23 August 2017

volume

55

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23 August 2017

issue

10

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23 August 2017

page(s)

639-648

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Newborn hearing screening--a silent revolution

23 August 2017

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss

21 January 2018

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21 January 2018

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High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects

21 January 2018

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The human alpha 2(XI) collagen gene (COL11A2): completion of coding information, identification of the promoter sequence, and precise localization within the major histocompatibility complex reveal overlap with the KE5 gene

21 January 2018

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Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

21 January 2018

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Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus

21 January 2018

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21 January 2018

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A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

21 January 2018

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A millennial myosin census

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Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.

21 January 2018

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MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.

21 January 2018

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A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family.

21 January 2018

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Radixin: cytoskeletal adopter and signaling protein

21 January 2018

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Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus

21 January 2018

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Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.

21 January 2018

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MicroRNAs: small RNAs with a big role in gene regulation

21 January 2018

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miRNA mutations are not a common cause of deafness.

21 January 2018

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Hereditary deafness and phenotyping in humans

21 January 2018

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Construction of a DNA chip for screening of genetic hearing loss

21 January 2018

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21 January 2018

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21 January 2018

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A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients

21 January 2018

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Connexins, connexons, and intercellular communication

21 January 2018

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7 January 2021

Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario

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7 January 2021

GJB2 mutations: passage through Iran

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7 January 2021

Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.

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7 January 2021

Identifiers

DOI

10.1038/JHG.2010.96

1 reference

23 August 2017

1 reference