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2017, First edition., Human diseases and conditions collection, ISBN 9781944749743, xii, 71 pages
Book
PLoS ONE, ISSN 1932-6203, 08/2015, Volume 10, Issue 8, pp. e0135088 - e0135088
Journal Article
Frontiers in cellular neuroscience, ISSN 1662-5102, 2015, Volume 9, p. 202
Hearing loss due to mutations in the connexin gene family, which encodes gap junctional proteins, is a common form of hereditary deafness. In particular,... 
Journal Article
Acta Oto-Laryngologica, ISSN 0001-6489, 05/2016, Volume 136, Issue 5, pp. 475 - 479
Objective To determine the incidence of congenital hearing loss (HL) in newborns by the rate of deafness-related genetic mutations. Design Clinical study of... 
genes | mass screening | Hearing loss | Mass screening | Genes | MOLECULAR ETIOLOGY | GJB2 | NONSYNDROMIC HEARING IMPAIRMENT | OTORHINOLARYNGOLOGY | PREVALENCE | SLC26A4 | CHINESE POPULATION | AGE | Cities - statistics & numerical data | Deafness - genetics | China | Humans | Female | Male | Mutation | Neonatal Screening | Infant, Newborn | Index Medicus
Journal Article
Clinical cancer research, ISSN 1078-0432, 2017, Volume 23, Issue 13, pp. 3325 - 3333
Journal Article
NUCLEIC ACIDS RESEARCH, ISSN 0305-1048, 2014, Volume 42, Issue 12, pp. 8039 - 8048
In this report, we investigated the molecular genetic mechanism underlying the deafness-associated mitochondrial tRNA(His) 12201T>C mutation. The... 
INHERITED HEARING-LOSS | OXIDATIVE STRESS | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRNA(SER(UCN)) GENE | NON-SYNDROMIC DEAFNESS | T7511C MUTATION | NONSYNDROMIC DEAFNESS | CHINESE FAMILY | CELLULAR BIOENERGETICS | DNA MUTATIONS | RIBOSOMAL-RNA MUTATION
Journal Article
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 04/2004, Volume 1011, Issue 1, pp. 259 - 271
Journal Article