'Behr syndrome' with OPA1 compound heterozygote mutations.
about
A neurodegenerative perspective on mitochondrial optic neuropathiesDysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations.Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophy.Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutationsReply: 'Behr syndrome' with OPA1 compound heterozygote mutations
P2860
'Behr syndrome' with OPA1 compound heterozygote mutations.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
'Behr syndrome' with OPA1 compound heterozygote mutations.
@en
'Behr syndrome' with OPA1 compound heterozygote mutations.
@nl
type
label
'Behr syndrome' with OPA1 compound heterozygote mutations.
@en
'Behr syndrome' with OPA1 compound heterozygote mutations.
@nl
prefLabel
'Behr syndrome' with OPA1 compound heterozygote mutations.
@en
'Behr syndrome' with OPA1 compound heterozygote mutations.
@nl
P2093
P2860
P50
P356
P1433
P1476
'Behr syndrome' with OPA1 compound heterozygote mutations.
@en
P2093
Bernd Wissinger
Claudia Zanna
Michele Carbonelli
Piero Barboni
Simone Schimpf
Teresa Rizza
P2860
P356
10.1093/BRAIN/AWU234
P407
P50
P577
2014-08-21T00:00:00Z