Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families.
about
Opa1 is required for proper mitochondrial metabolism in early developmentThe Interplay between Oncogenic Signaling Networks and Mitochondrial Dynamics.A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese familyThe clinical maze of mitochondrial neurologyDisturbed mitochondrial dynamics and neurodegenerative disorders.Diagnostic genetic testing for patients with bilateral optic neuropathy and comparison of clinical features according to OPA1 mutation status.Processing of OPA1 with a novel N-terminal mutation in patients with autosomal dominant optic atrophy: Escape from nonsense-mediated decay.Mitochondrial dynamics as regulators of cancer biology.Mitochondrial-Based Therapeutics for the Treatment of Spinal Cord Injury: Mitochondrial Biogenesis as a Potential Pharmacological Target.
P2860
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P2860
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Optic atrophy plus phenotype d ...... ne: two more Italian families.
@ast
Optic atrophy plus phenotype d ...... ne: two more Italian families.
@en
type
label
Optic atrophy plus phenotype d ...... ne: two more Italian families.
@ast
Optic atrophy plus phenotype d ...... ne: two more Italian families.
@en
prefLabel
Optic atrophy plus phenotype d ...... ne: two more Italian families.
@ast
Optic atrophy plus phenotype d ...... ne: two more Italian families.
@en
P2093
P2860
P50
P1476
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families
@en
P2093
Alessandra Cosi
Andreina Bordoni
Giulietta Riboldi
Irene Colombo
Maura Servida
Maurizio Moggio
Michela Ranieri
Roberto Del Bo
P2860
P304
P356
10.1016/J.JNS.2011.12.002
P577
2011-12-22T00:00:00Z