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Gene expression and functional analysis of GJB2 mutated HaCaT cell lines [D66H]

ABSTRACT: Vohwinkel syndrome, VS (OMIM#124500), a rare autosomal dominant genetic disease, with less than 50 reported cases in the literature. Although clinical symptoms of VS are complex, which are caused by GJB2 mutation is more typical. To explore related differential genes and signaling pathways of Vohwinkel syndrome (VS) caused by mutations of GJB2. Human Gene Expression Array of two types of GJB2-VS mutated (G130V and D66H) HaCaT cell lines and identified distinct classes of up- and down- regulated genes during this process.

ORGANISM(S): Homo sapiens

PROVIDER: GSE200386 | GEO | 2023/09/30

REPOSITORIES: GEO

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Gene expression and functional analysis of GJB2 mutated HaCaT cell lines [G130V]

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