Characterization of a rare Unverricht-Lundborg disease mutation.
about
Putative alternative functions of human stefin B (cystatin B): binding to amyloid-beta, membranes, and copper.Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy.Correction of a Splicing Mutation Affecting an Unverricht-Lundborg Disease Patient by Antisense Therapy
P2860
Characterization of a rare Unverricht-Lundborg disease mutation.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Characterization of a rare Unverricht-Lundborg disease mutation.
@ast
Characterization of a rare Unverricht-Lundborg disease mutation.
@en
type
label
Characterization of a rare Unverricht-Lundborg disease mutation.
@ast
Characterization of a rare Unverricht-Lundborg disease mutation.
@en
prefLabel
Characterization of a rare Unverricht-Lundborg disease mutation.
@ast
Characterization of a rare Unverricht-Lundborg disease mutation.
@en
P2860
P50
P1476
Characterization of a rare Unverricht-Lundborg disease mutation.
@en
P2093
Ana Joana Duarte
P2860
P356
10.1016/J.YMGMR.2015.07.005
P577
2015-08-05T00:00:00Z