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Article

Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia.

The British journal of dermatology - 1 Sept 2018

Intarak N, Theerapanon T, Srijunbarl A, Suphapeetiporn K, Porntaveetus T, Shotelersuk V

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Share to Ectodermal Dysplasia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 29526031
DOI: 10.1111/bjd.16541

Genes

KREMEN1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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