Novel and recurrent C1 inhibitor gene mutations in nine Japanese patients with hereditary angioedema.

Iwamoto, Kazumasa; Tanaka, Akio; Hiragun, Makiko; Kawai, Mikio; Mihara, Shoji; Takenaka, Motoi; Shibuya, Michiko; Inomata, Naoko; Hatano, Yutaka; Shimizu, Fumiaki; Kousaka, Takao; Hide, Michihiro

Iwamoto, Kazumasa; Tanaka, Akio; Hiragun, Makiko; Kawai, Mikio; Mihara, Shoji; Takenaka, Motoi; Shibuya, Michiko; Inomata, Naoko; Hatano, Yutaka; Shimizu, Fumiaki; Kousaka, Takao; Hide, Michihiro.

J Dermatol Sci ; 68(1): 68-70, 2012 Oct.

Article in En | MEDLINE | ID: mdl-22831796

Subject(s)

Angioedemas, Hereditary/genetics; Complement C1 Inactivator Proteins/genetics; Mutation; Adult; Aged; Angioedemas, Hereditary/blood; Angioedemas, Hereditary/ethnology; Angioedemas, Hereditary/therapy; Asian People/genetics; Complement C1 Inactivator Proteins/analysis; Complement C1 Inhibitor Protein; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Japan; Male; Middle Aged; Phenotype; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Complement C1 Inactivator Proteins / Angioedemas, Hereditary / Mutation Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: J Dermatol Sci Journal subject: DERMATOLOGIA Year: 2012 Document type: Article Country of publication: Netherlands

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