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
No abstract is available from the source.
Topics
- Arachidonate 12-Lipoxygenase
- Female
- Homozygote
- Humans
- Ichthyosiform Erythroderma, Congenital
- Infant
- Mutation, Missense
- Phenotype