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.
about
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.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh-hant
name
Molecular analysis of afibrino ...... el FGA c.54+3A>C substitution.
@en
Molecular analysis of afibrino ...... el FGA c.54+3A>C substitution.
@nl
type
label
Molecular analysis of afibrino ...... el FGA c.54+3A>C substitution.
@en
Molecular analysis of afibrino ...... el FGA c.54+3A>C substitution.
@nl
prefLabel
Molecular analysis of afibrino ...... el FGA c.54+3A>C substitution.
@en
Molecular analysis of afibrino ...... el FGA c.54+3A>C substitution.
@nl
P2093
P2860
P1476
Molecular analysis of afibrino ...... el FGA c.54+3A>C substitution.
@en
P2093
Aiko Tanaka
Fumiko Terasawa
Kazuyuki Matsuda
Keigo Kainuma
Mitsuhiro Fujiwara
Mitsutoshi Sugano
Nobuo Okumura
Yuka Takezawa
P2860
P2888
P356
10.1007/S12185-012-1100-3
P577
2012-05-26T00:00:00Z