A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss-Reference-Cited by-同舟云学术

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A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss

Published:2019-04-11 Issue:4 Volume:14 Page:e0215212
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Liu Yalan^ORCID,Hu Chang,Liu Chang,Liu Deyuan,Mei Lingyun,He Chufeng,Jiang Lu,Wu Hong,Chen Hongsheng,Feng Yong

Funder

the National Basic Research Program of China

the China Postdoctoral Science Foundation

the Nature Science Foundation of Hunan province

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference34 articles.

1. International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient;BJ Liming;Int J Pediatr Otorhinolaryngol,2016

2. Molecular diagnostics for hereditary hearing loss in children;M Sommen;Expert Rev Mol Diagn,2017

3. Genetic epidemiological studies of congenital/prelingual deafness in Turkey: population structure and mating type are major determinants of mutation identification;M Tekin;Am J Med Genet A,2007

4. Genetics of hearing and deafness;S Angeli;Anat Rec (Hoboken),2012

5. Whole-exome sequencing to decipher the genetic heterogeneity of hearing loss in a Chinese family with deaf by deaf mating;J Qing;PLoS One,2014

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