about
Multi-system neurological disease is common in patients with OPA1 mutationsIdentification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping.OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules.Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.Down-regulation of OPA1 in patients with primary open angle glaucomaCorrelation between polymorphisms in the MFN1 gene and myopia in Chinese population.Inherited mitochondrial optic neuropathies.The investigation on the role of mitochondrial fusion protein 1 in the development of myopiaAUTOPHAGY, MITOCHONDRIAL DYNAMICS AND RETINAL DISEASES.Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies.Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophy.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Focus on molecules: the OPA1 protein.
@ast
Focus on molecules: the OPA1 protein.
@en
type
label
Focus on molecules: the OPA1 protein.
@ast
Focus on molecules: the OPA1 protein.
@en
prefLabel
Focus on molecules: the OPA1 protein.
@ast
Focus on molecules: the OPA1 protein.
@en
P1476
Focus on molecules: the OPA1 protein
@en
P2093
Vanessa Davies
P304
P356
10.1016/J.EXER.2005.11.021
P577
2006-03-23T00:00:00Z