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t/gene-gja1

GJA1 gene

Discuss publications and research concerning the GJA1 gene.

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Related literature

Hypoxia Modulates Nanovesicle Phenotype and Angiogenic Function From Human Pluripotent Stem Cells.
GJA1
The evolving genetic landscape of ILVEN: A comprehensive review.
GJA1
Astroglial toxicity promotes synaptic degeneration in the thalamocortical circuit in frontotemporal dementia with GRN mutations.
GJA1
Novel Myopia Genes and Pathways Identified From Syndromic Forms of Myopia.
GJA1
Inflammatory Linear Verrucous Epidermal Nevus with a Postzygotic GJA1 Mutation Is a Mosaic Erythrokeratodermia Variabilis et Progressiva.
GJA1
Erythrokeratodermia variabilis et progressiva.
GJA1
Mutations in MicroRNA Genes and Their Binding Sites are Infrequently Associated with Human Colorectal Cancer in the Kashmiri Population.
GJA1
Novel mutation p.Gly59Arg in GJB6 encoding connexin 30 underlies palmoplantar keratoderma with pseudoainhum, knuckle pads and hearing loss.
GJA1
GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype.
GJA1
Gene symbol: GJA1. Disease: oculodentodigital dysplasia.
GJA1

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