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Emopamil Binding Protein Mutation in Conradi-Hünermann-Happle Syndrome Representing Plaque-Type Psoriasis

Conradi-Hünermann-Happle syndrome (CDPX2, OMIM 302960) is an inherited X-linked dominant variant of chondrodysplasia punctata which primarily affects the skin, bones, and eyes. CDPX2 patients display skin defects, including ichthyotic lesions, follicular atrophoderma, cicatricial alopecia, and less...

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Detaylı Bibliyografya
Yayımlandı:Indian J Dermatol
Asıl Yazarlar: Ozyurt, Kemal, Subasioglu, Asli, Ozturk, Perihan, Inci, Rahime, Ozkan, Fuat, Bueno, Elena, Cañueto, Javier, González Sarmiento, Rogelio
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2015
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4372958/
https://ncbi.nlm.nih.gov/pubmed/25814754
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.152570
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