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Article

Progressive Nagashima-type palmoplantar keratosis in a Chinese patient with recurrent c.796C>T mutation in SERPINB7.

Indian journal of dermatology, venereology and leprology - 1 Jan 2000

Qiu Meng, Zou Xian-Biao

Abstract excerpt

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Share to Asian People
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27506501
DOI: 10.4103/0378-6323.187093

Genes

SERPINB7

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

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Progressive Nagashima-type palmoplantar keratosis in a Chinese patient with recurrent c.796C>T mutation in SERPINB7.PMID 27506501Read ↗

Nagashima-type palmoplantar keratosis caused by compound heterozygous mutations in SERPINB7.Semantic proximity Read ↗

A sporadic case of Nagashima-type palmoplantar keratosis caused by gene mutation in SERPINB7.Semantic proximity Read ↗

Two novel mutations of SERPINB7 in eight cases of Nagashima-type palmoplantar keratosis in the Chinese population.Semantic proximity Read ↗

Identification of previously unknown SERPINB7 splice variants in patients with Nagashima-type palmoplantar keratosis reveals the importance of the CD-loop of SERPINB7.Semantic proximity Read ↗

Nagashima-type palmoplantar keratosis in a Chinese Han population.Semantic proximity Read ↗

Nagashima-type palmoplantar keratosis in Finland caused by a SERPINB7 founder mutationSemantic proximity Read ↗

Nagashima-type palmoplantar keratosis: a common Asian type caused by SERPINB7 protease inhibitor deficiency.Semantic proximity Read ↗

Potential digenic inheritance of SERPINB7 and SERPINA12 variants in Chinese patients with Nagashima-type palmoplantar keratosisSemantic proximity Read ↗

Investigation of Nagashima-type palmoplantar keratoderma in China: A cross-sectional study of 234 patients.Semantic proximity Read ↗

Mutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosis.Semantic proximity Read ↗

A heterozygous SERPINB7 mutation is a possible modifying factor for epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

Three new founder mutations in Chinese patients with Nagashima-type palmoplantar keratodermaSemantic proximity Read ↗

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