Human iPSC disease modelling reveals functional and structural defects in retinal pigment epithelial cells harbouring the m.3243A > G mitochondrial DNA mutation.
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Human iPSC disease modelling reveals functional and structural defects in retinal pigment epithelial cells harbouring the m.3243A > G mitochondrial DNA mutation.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Human iPSC disease modelling r ...... G mitochondrial DNA mutation.
@en
Human iPSC disease modelling r ...... G mitochondrial DNA mutation.
@nl
type
label
Human iPSC disease modelling r ...... G mitochondrial DNA mutation.
@en
Human iPSC disease modelling r ...... G mitochondrial DNA mutation.
@nl
prefLabel
Human iPSC disease modelling r ...... G mitochondrial DNA mutation.
@en
Human iPSC disease modelling r ...... G mitochondrial DNA mutation.
@nl
P2093
P2860
P50
P1433
P1476
Human iPSC disease modelling r ...... > G mitochondrial DNA mutation
@en
P2093
Adriana Buskin
Dean Hallam
Joseph Collin
Patrick Yu-Wai-Man
P2860
P2888
P356
10.1038/S41598-017-12396-2
P407
P577
2017-09-26T00:00:00Z