A case of a Japanese neonate with congenital ichthyosiform erythroderma diagnosed as Netherton syndrome. [electronic resource]
Producer: 20070208Description: 677-80 p. digitalISSN:- 0307-6938
- Carrier Proteins -- genetics
- DNA Mutational Analysis
- Exons
- Female
- Gene Deletion
- Hair -- abnormalities
- Humans
- Ichthyosiform Erythroderma, Congenital -- genetics
- Infant, Newborn
- Proteinase Inhibitory Proteins, Secretory
- Serine Peptidase Inhibitor Kazal-Type 5
- Serine Proteinase Inhibitors -- genetics
- Syndrome
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Publication Type: Case Reports; Journal Article
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