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Mapping of epidermolysis bullosa simplex mutation to chromosome 12.

Epidermolysis bullosa simplex (EBS) is a dominantly inherited genodermatosis characterized by intraepidermal blister formation. Recent reports have suggested that EBS mutations may relate to keratin abnormalities. In this study, we conducted RFLP analyses to test the hypothesis that EBS is linked to...

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Detaylı Bibliyografya
Asıl Yazarlar: Ryynänen, M, Knowlton, R G, Uitto, J
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1991
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683248/
https://ncbi.nlm.nih.gov/pubmed/1718160
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