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GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss Cover

GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss

Revista Romana de Medicina de Laborator
Volume 25 (2017): Issue 1 (January 2017)
By: Călin Lazăr,  Radu Popp,  Camelia Al-Khzouz,  Gheorghe Mihuț and  Paula Grigorescu-Sido  
Open Access
|Feb 2017

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DOI: https://doi.org/10.1515/rrlm-2017-0004 | Journal eISSN: 2284-5623 | Journal ISSN: 1841-6624
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Language: English
Page range: 37 - 46
Submitted on: Aug 30, 2016
Accepted on: Nov 29, 2016
Published on: Feb 18, 2017
Published by: Romanian Association of Laboratory Medicine
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Keywords:
connexin 26 and 30,
GJB2 mutation,
GJB6 mutation,
sensorineural hearing loss
Related subjects:
Life sciences,
Molecular biology,
Biochemistry,
Human biology,
Microbiology and virology

© 2017 Călin Lazăr, Radu Popp, Camelia Al-Khzouz, Gheorghe Mihuț, Paula Grigorescu-Sido, published by Romanian Association of Laboratory Medicine
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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