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Article

A severe collodion phenotype in the newborn period associated with a homozygous missense mutation in ALOX12B.

The British journal of dermatology - 1 Jul 2015

Bland P J, Chronnell C, Plagnol V, Kayserili H, Kelsell D P

Abstract excerpt

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Share to Arachidonate 12-Lipoxygenase
Share to Homozygote
Share to Ichthyosiform Erythroderma, Congenital
Share to Infant

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation, Missense

Share to Phenotype

Source

Identifiers

PMID: 25524567
DOI: 10.1111/bjd.13627

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Related research

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A severe collodion phenotype in the newborn period associated with a homozygous missense mutation in ALOX12B.PMID 25524567Read ↗

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