Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A>C substitution

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概要

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2012-07-01

著者

Terasawa Fumiko
Shinshu Univ. Jpn
Terasawa Fumiko
Department Of Biomedical Laboratory Sciences School Of Health Sciences Shinshu University
Okumura Nobuo
Shinshu Univ. Jpn
OKUMURA Nobuo
Department of Biomedical Laboratory Sciences, School of Health Sciences, Shinshu University
Fujiwara Mitsuhiro
Department Of Pediatrics And Department Of Hematology/oncology Kurashiki Central Hospital
Sugano Mitsutoshi
Department Of Laboratory Medicine Shinshu University School Of Medicine
Matsuda Kazuyuki
Department Of Internal Medicine Yamaguchi Prefecture General Hospital
TAKEZAWA Yuka
Department of Health and Medical Sciences, Graduate School of Medicine, Shinshu University
TANAKA Aiko
Department of Pediatrics, Kurashiki Central Hospital
KAINUMA Keigo
Department of Pediatrics, Mie Prefectural Medical Center Hospital
Takezawa Yuka
Department Of Health And Medical Sciences Graduate School Of Medicine Shinshu University
Kainuma Keigo
Department Of Pediatrics Mie Prefectural Medical Center Hospital
Okumura Nobuo
Department Of Health And Medical Sciences Graduate School Of Medicine Shinshu University
Tanaka Aiko
Department Of Pediatrics Kurashiki Central Hospital
Okumura Nobuo
Department Of Biomedical Laboratory Sciences School Of Health Sciences Shinshu University
Sugano Mitsutoshi
Department Of Laboratory Medicine Shinshu University Hospital
MATSUDA Kazuyuki
Department of Laboratory Medicine, Shinshu University Hospital
Tanaka Aiko
Department of Medicine, Shiga University of Medical Science

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