Futatani Takeshi | Department Of Pediatrics Faculty Of Medicine University Of Toyama

スポンサーリンク

概要

関連著者

もっと見る

著作論文

ブルトン・チロシン・キナーゼの第1イントロンにおける転写調節異常
Genetic Analysis in Patients with Left Ventricular Noncompaction and Evidence for Genetic Heterogeneity(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
OE-269 Evidence of Genetic Heterogeneity in Left Ventricular Noncompaction(Cardiomyopathy, basic/clinical-1 (M) OE45,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan
Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease
PE-306 SCN5A Variant in Japanese Patients with Left Ventricular Noncompaction and Arrhythmia(Cardiomyopathy, basic/clinical-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
Mutational Analysis of the WASP Gene in 2 Korean Families with Wiskott-Aldrich Syndrome
Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements resulting in large deletion, in Korean X-linked agammaglobulinemia patients
Atypical X-linked Agammaglobulinemia Diagnosed in Three Adult
Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia
A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes

もっと見る

スポンサーリンク