Molecular Mechanisms of Type II Factor XIII Deficiency: Novel Gly562-Arg Mutation and C-Terminal Truncation of the A Subunit Cause Factor XIII Deficiency as Characterized in a Mammalian Expression System期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Molecular Mechanisms of Type II Factor XIII Deficiency: Novel Gly562-Arg Mutation and C-Terminal Truncation of the A Subunit Cause Factor XIII Deficiency as Characterized in a Mammalian Expression System

Authors:	Takahashi, Nobumasa Tsukamoto, Hiroaki Umeyama, Hideaki Castaman, Giancarlo Rodeghiero, Francesco Ichinose, Akitada

Affiliation:	From the Department of Molecular Patho-Biochemistry, YamagataUniversity School of Medicine, Yamagata, Japan; the Department ofPhysical Chemistry, Kitasato University School of PharmaceuticalSciences, Tokyo, Japan; the Department of Haematology, San BortoloHospital, Vicenza, Italy.

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