The prevalent deep intronic c. 639+919 G>A GLA mutation causes pseudoexon activation and Fabry disease by abolishing the binding of hnRNPA1 and hnRNP A2/B1 to a splicing silencer.
about
The prevalent deep intronic c. 639+919 G>A GLA mutation causes pseudoexon activation and Fabry disease by abolishing the binding of hnRNPA1 and hnRNP A2/B1 to a splicing silencer.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
The prevalent deep intronic c. ...... A2/B1 to a splicing silencer.
@en
type
label
The prevalent deep intronic c. ...... A2/B1 to a splicing silencer.
@en
prefLabel
The prevalent deep intronic c. ...... A2/B1 to a splicing silencer.
@en
P2093
P50
P1476
The prevalent deep intronic c. ...... P A2/B1 to a splicing silencer
@en
P2093
Bruno Palhais
Gitte Hoffmann Bruun
Kira S Nielsen
P304
P356
10.1016/J.YMGME.2016.08.007
P577
2016-08-27T00:00:00Z