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Article

A Novel NCSTN Gene Mutation in a Japanese Family with Hidradenitis Suppurativa.

Acta dermato-venereologica - 6 Oct 2020

Nishimori Nobuyuki, Hayama Koremasa, Kimura Kumiko, Fujita Hideki, Fujiwara Kyoko, Terui Tadashi

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PMID: 32926179
DOI: 10.2340/00015555-3632
PMCID: PMC9274921

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Related research

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A Novel NCSTN Gene Mutation in a Japanese Family with Hidradenitis Suppurativa.PMID 32926179Read ↗

A novel NCSTN mutation alone may be insufficient for the development of familial hidradenitis suppurativaSemantic proximity Read ↗

A novel c.671_682del NCSTN variant in a family with hidradenitis suppurativa: a pilot study.Semantic proximity Read ↗

A Novel NCSTN Mutation in a Three-Generation Chinese Family with Hidradenitis Suppurative.Semantic proximity Read ↗

Characterization of a Novel Mutation in the NCSTN Gene in a Large Chinese Family with Acne Inversa.Semantic proximity Read ↗

Genetic analysis of <i> <scp>NCSTN</scp> </i> for potential association with hidradenitis suppurativa in familial and nonfamilial patientsSemantic proximity Read ↗

Confirmation by Exome Sequencing of the Pathogenic Role of NCSTN Mutations in Acne Inversa (Hidradenitis Suppurativa)Semantic proximity Read ↗

A novel splice site mutation in NCSTN underlies a Japanese family with hidradenitis suppurativa.Semantic proximity Read ↗

A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization diseaseSemantic proximity Read ↗

Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome.Semantic proximity Read ↗

A loss-of-function NCSTN mutation associated with familial Dowling Degos disease and hidradenitis suppurativa.Semantic proximity Read ↗

A novel insertion mutation of CDSN responsible for hypotrichosis simplex of scalp in a Chinese family.Semantic proximity Read ↗

Increased expression profile of NCSTN, Notch and PI3K/AKT3 in hidradenitis suppurativaSemantic proximity Read ↗

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