Literature DB >> 21542834

DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment.

M A Tabatabaiefar, F Alasti, L Shariati, E Farrokhi, E Fransen, M R Nooridaloii, M H Chaleshtori, G Van Camp.   

Abstract

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Year:  2011        PMID： 21542834     DOI： 10.1111/j.1399-0004.2010.01593.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  8 in total

Review 1.  Voltage-Gated Calcium Channels: Key Players in Sensory Coding in the Retina and the Inner Ear.

Authors:  Tina Pangrsic; Joshua H Singer; Alexandra Koschak
Journal:  Physiol Rev       Date:  2018-10-01       Impact factor: 37.312

Review 2.  ARNSHL gene identification: past, present and future.

Authors:  Ayesha Imtiaz
Journal:  Mol Genet Genomics       Date:  2022-07-23       Impact factor: 2.980

3.  Ca2+-binding protein 2 inhibits Ca2+-channel inactivation in mouse inner hair cells.

Authors:  Maria Magdalena Picher; Anna Gehrt; Sandra Meese; Aleksandra Ivanovic; Friederike Predoehl; SangYong Jung; Isabelle Schrauwen; Alberto Giulio Dragonetti; Roberto Colombo; Guy Van Camp; Nicola Strenzke; Tobias Moser
Journal:  Proc Natl Acad Sci U S A       Date:  2017-02-09       Impact factor: 11.205

4.  A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment.

Authors:  Isabelle Schrauwen; Sarah Helfmann; Akira Inagaki; Friederike Predoehl; Mohammad Amin Tabatabaiefar; Maria Magdalena Picher; Manou Sommen; Celia Zazo Seco; Jaap Oostrik; Hannie Kremer; Annelies Dheedene; Charlotte Claes; Erik Fransen; Morteza Hashemzadeh Chaleshtori; Paul Coucke; Amy Lee; Tobias Moser; Guy Van Camp
Journal:  Am J Hum Genet       Date:  2012-09-13       Impact factor: 11.025

Review 5.  Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future.

Authors:  Anushree Acharya; Isabelle Schrauwen; Suzanne M Leal
Journal:  Hum Genet       Date:  2021-07-22       Impact factor: 4.132

6.  Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations.

Authors:  Marzieh Naseri; Masoud Akbarzadehlaleh; Marjan Masoudi; Najmeh Ahangari; Ali Akbar Poursadegh Zonouzi; Ahmad Poursadegh Zonouzi; Leila Shams; Azim Nejatizadeh
Journal:  Iran J Public Health       Date:  2018-01       Impact factor: 1.429

7.  Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations.

Authors:  Mahbobeh Koohiyan; Somayeh Reiisi; Fatemeh Azadegan-Dehkordi; Mansoor Salehi; Hamidreza Abtahi; Morteza Hashemzadeh-Chaleshtori; Mohammad Reza Noori-Daloii; Mohammad Amin Tabatabaiefar
Journal:  Iran J Public Health       Date:  2019-09       Impact factor: 1.429

8.  Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss.

Authors:  Ma Tabatabaiefar; F Alasti; M Montazer Zohour; L Shariati; E Farrokhi; Dd Farhud; Gv Camp; Mr Noori-Daloii; M Hashemzadeh Chaleshtori
Journal:  Iran J Public Health       Date:  2011-06-30       Impact factor: 1.429
  8 in total

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