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Article

A missense mutation in KRT14 causing a dermatopathia pigmentosa reticularis/Naegeli-Franceschetti-Jadassohn phenotype.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Sept 2010

van Steensel M A M, Lemmink H H

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Share to Abnormalities, Multiple
Share to Hyperpigmentation
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 20180888
DOI: 10.1111/j.1468-3083.2010.03598.x

Genes

KRT14

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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A missense mutation in KRT14 causing a dermatopathia pigmentosa reticularis/Naegeli-Franceschetti-Jadassohn phenotype.PMID 20180888Read ↗

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