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t/gene-gjb2

GJB2 gene

Discuss publications and research concerning the GJB2 gene.

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Related literature

Spectrum of DNA Variants Underlying Deafness in an Ecuadorian Cohort.
GJB2
Natural history and phenotype-genotype correlations in GJB2-related hearing loss: a systematic and comprehensive review.
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Prevalence of GJB2 gene mutations in nonsyndromic hearing impairments: A systematic review and meta-analysis.
GJB2
Connexin 26 in Hearing Health and Disease: StructuralFoundations, Mutation Mechanisms, and Therapeutic Perspectives.
GJB2
Peculiar Phenotype of Linear Prepubertal Hidradenitis Suppurativa Associated With Trisomy 13: Report of Two Clinical Cases.
GJB2
Regulatory mechanisms of connexin26.
GJB2
Ocular phenotype and therapeutic interventions in keratitis-ichthyosis-deafness (KID) syndrome.
GJB2
Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss.
GJB2
Common and Founder Mutations for Monogenic Traits in Sub-Saharan African Populations.
GJB2
STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population.
GJB2

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