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Article

Hailey-Hailey disease due to ATP2C1 splice site mutation, successfully treated with minocycline hydrochloride.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Jan 2018

Kono M, Niizawa M, Takeichi T, Muro Y, Akiyama M

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Share to Aged, 80 and over
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Share to Calcium-Transporting ATPases
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 28653466
DOI: 10.1111/jdv.14439

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Hailey-Hailey disease due to ATP2C1 splice site mutation, successfully treated with minocycline hydrochloride.PMID 28653466Read ↗

A case of Hailey-Hailey disease with novel ATP2C1 gene variant (c.G925C) showing unusual phenotype.Semantic proximity Read ↗

Mild Hailey-Hailey disease cases with aberrant splicing variants of ATP2C1 successfully controlled with excimer light.Semantic proximity Read ↗

Mild case of Hailey-Hailey disease caused by a novel ATP2C1 mutation.Semantic proximity Read ↗

Hailey–Hailey Disease: Identification of Novel Mutations in ATP2C1 and Effect of Missense Mutation A528P on Protein Expression LevelsSemantic proximity Read ↗

A novel missense mutation of the ATP2C1 gene in a Chinese patient with Hailey–Hailey diseaseSemantic proximity Read ↗

Novel missense mutation (A414P) in ATP2C1 in a case of familial Hailey-Hailey disease.Semantic proximity Read ↗

Diagnosis of Hailey-Hailey disease facilitated by DNA testing: a novel mutation in ATP2C1.Semantic proximity Read ↗

A novel deletion mutation in the ATP2C1 gene in a case of generalized Hailey-Hailey disease possibly aggravated by scabies infection.Semantic proximity Read ↗

Two patients with Hailey-Hailey disease with novel pathogenic ATP2C1 variants suggesting possible genotype/phenotype correlations.Semantic proximity Read ↗

Identification of 2 Novel Mutations in ATP2C1 Gene in Hailey-Hailey Disease and a Literature Review of Variations in a Chinese Han Population.Semantic proximity Read ↗

Hailey-Hailey Disease Caused by a Novel Deep Intronic Variant in ATP2C1.Semantic proximity Read ↗

Hailey-Hailey disease with a novel variant, c.1978dupG, in the ATP2C1 gene.Semantic proximity Read ↗

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