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M Votruba

Showing results (21-30 of 29) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|October 26, 1999
Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qterG E Holder, M Votruba, A C Carter, et al.
Cell Death & Disease|July 30, 2016
Mitochondrial dysfunction in an Opa1(Q285STOP) mouse model of dominant optic atrophy results from Opa1 haploinsufficiencyY Kushnareva, Y Seong, A Y Andreyev, et al.
Neuroradiology|April 20, 2000
MRI of the intraorbital optic nerve in patients with autosomal dominant optic atrophyM Votruba, S Leary, N Losseff, et al.
Human Genetics|December 6, 2001
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effectD L Thiselton, C Alexander, A Morris, et al.
Mitochondrion|July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathyA Majander, A G Robson, C João, et al.
Development (Cambridge, England)|February 24, 2009
An essential role for the RNA-binding protein Smaug during the Drosophila maternal-to-zygotic transitionBeatrice Benoit, Chun Hua He, Fan Zhang, et al.
Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Cell|November 24, 2001
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye developmentY Gong, R B Slee, N Fukai, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Documenta Ophthalmologica. Advances in Ophthalmology|October 26, 1999
Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qterG E Holder, M Votruba, A C Carter, et al.
Cell Death & Disease|July 30, 2016
Mitochondrial dysfunction in an Opa1(Q285STOP) mouse model of dominant optic atrophy results from Opa1 haploinsufficiencyY Kushnareva, Y Seong, A Y Andreyev, et al.
Neuroradiology|April 20, 2000
MRI of the intraorbital optic nerve in patients with autosomal dominant optic atrophyM Votruba, S Leary, N Losseff, et al.
Human Genetics|December 6, 2001
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effectD L Thiselton, C Alexander, A Morris, et al.
Mitochondrion|July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathyA Majander, A G Robson, C João, et al.
Development (Cambridge, England)|February 24, 2009
An essential role for the RNA-binding protein Smaug during the Drosophila maternal-to-zygotic transitionBeatrice Benoit, Chun Hua He, Fan Zhang, et al.
Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Cell|November 24, 2001
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye developmentY Gong, R B Slee, N Fukai, et al.
Pageof 3