Identification of 5 novel germline APC mutations and characterization of clinical phenotypes in Japanese patients with classical and attenuated familial adenomatous polyposis

BACKGROUND: Familial adenomatous polyposis (FAP) is an autosomal dominant hereditary disease characterized by multiple colorectal adenomatous polyps and frequent extracolonic manifestations. An attenuated form of FAP (AFAP) is diagnosed based on a milder colorectal phenotype, and the colorectal phen...

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Detaylı Bibliyografya
Asıl Yazarlar: Tao, Hong, Shinmura, Kazuya, Yamada, Hidetaka, Maekawa, Masato, Osawa, Satoshi, Takayanagi, Yasuhiro, Okamoto, Kazuya, Terai, Tomohiro, Mori, Hiroki, Nakamura, Toshio, Sugimura, Haruhiko
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2010
Konular:
Short Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2994888/
https://ncbi.nlm.nih.gov/pubmed/21078199
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0500-3-305
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