Epidemiological study of nonsyndromic hearing loss in Sicilian newborns
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference34 articles.
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2. Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness
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1. The Frequency of Common Deafness-Associated Variants Among 3,555,336 Newborns in China and 141,456 Individuals Across Seven Populations Worldwide;Ear & Hearing;2022-09-23
2. Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden;Life;2020-10-28
3. Prevalence of Deafness-Associated Connexin-26 (GJB2) and Connexin-30 (GJB6) Pathogenic Alleles in a Large Patient Cohort from Eastern Sicily;Annals of Human Genetics;2015-06-19
4. Distribution and phenotype ofGJB2mutations in 102 Sicilian patients with congenital non syndromic sensorineural hearing loss;International Journal of Audiology;2014-05-05
5. A genotype–phenotype correlation in Sicilian patients with GJB2 biallelic mutations;European Archives of Oto-Rhino-Laryngology;2014-03-14
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