SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency.
about
SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency.
description
2018 nî lūn-bûn
@nan
2018年の論文
@ja
2018年学术文章
@wuu
2018年学术文章
@zh-cn
2018年学术文章
@zh-hans
2018年学术文章
@zh-my
2018年学术文章
@zh-sg
2018年學術文章
@yue
2018年學術文章
@zh
2018年學術文章
@zh-hant
name
SCO2 mutations cause early-ons ...... th cellular copper deficiency.
@en
SCO2 mutations cause early-ons ...... th cellular copper deficiency.
@nl
type
label
SCO2 mutations cause early-ons ...... th cellular copper deficiency.
@en
SCO2 mutations cause early-ons ...... th cellular copper deficiency.
@nl
prefLabel
SCO2 mutations cause early-ons ...... th cellular copper deficiency.
@en
SCO2 mutations cause early-ons ...... th cellular copper deficiency.
@nl
P2093
P2860
P50
P356
P1433
P1476
SCO2 mutations cause early-ons ...... th cellular copper deficiency.
@en
P2093
Adriana P Rebelo
Amjad Farooq
Carlos T Moraes
Diana Mnatsakanova
Dimah Saade
Eric A Schon
Kathy Mathews
Lisa Abreu
Tyler C Huff
P2860
P356
10.1093/BRAIN/AWX369
P407
P577
2018-01-16T00:00:00Z