Oncostatin M Receptor-β Mutations Underlie Familial Primary Localized Cutaneous Amyloidosis

Familial primary localized cutaneous amyloidosis (FPLCA) is an autosomal-dominant disorder associated with chronic skin itching and deposition of epidermal keratin filament-associated amyloid material in the dermis. FPLCA has been mapped to 5p13.1–q11.2, and by candidate gene analysis, we identified...

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Detalhes bibliográficos
Main Authors: Arita, Ken, South, Andrew P., Hans-Filho, Günter, Sakuma, Thais Harumi, Lai-Cheong, Joey, Clements, Suzanne, Odashiro, Maçanori, Odashiro, Danilo Nakao, Hans-Neto, Günter, Hans, Nelise Ritter, Holder, Maxine V., Bhogal, Balbir S., Hartshorne, Sian T., Akiyama, Masashi, Shimizu, Hiroshi, McGrath, John A.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Human Genetics 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2253984/
https://ncbi.nlm.nih.gov/pubmed/18179886
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2007.09.002
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