Add to ORKGnone12noneC. Tonon; R. Lodi; D. N. Manners; E. Malucelli; C. Testa; M. L. Valentino; P. Barboni; S. Schaich; S. Schimpf; B. Wissinger; B. Barbiroli; V. CarelliC. Tonon; R. Lodi; D. N. Manners; E. Malucelli; C. Testa; M. L. Valentino; P. Barboni; S. Schaich; S. Schimpf; B. Wissinger; B. Barbiroli; V. Carell
Optic atrophy (OA) with autosomal inheritance is a form of optic neuropathy characterized by the pro...
Autosomal dominant optic atrophy (ADOA) is a slowly progressive ocular disorder associated with reti...
Purpose: Retinal ganglion cells (RGCs) are susceptible to mitochondrial deficits and also the major ...
none13noneLODI R; TONON C; VALENTINO ML; IOTTI S; CLEMENTI V; MALUCELLI E; BARBONI P; LONGANESI L; S...
Autosomal Dominant Optic Atrophy (ADOA) is the most common inherited optic atrophy where vision impa...
Mutations in the OPA1 gene product result in the most common form of autosomal dominant optic atroph...
none13noneZanna C.; Ghelli A.; Porcelli A.M.; Karbowski M.; Youle R.J.; Schimpf S.; Wissinger B.; Pi...
Autosomal dominant optic atrophy (ADOA) is a progressive ophthalmologic disorder caused in two-third...
The aim of this study was to determine the pathogenetic mechanism of autosomal dominant optic atroph...
To characterize the molecular links between type-1 autosomal dominant optic atrophy (ADOA) and OPA1 ...
International audienceThe OPA1 gene, encoding a dynamin-like mitochondrial GTPase, is involved in au...
Autosomal dominant optic atrophy (ADOA), the commonest cause of inherited optic atrophy, is caused b...
AbstractAutosomal Dominant Optic Atrophy (ADOA) is characterized by the selective degeneration of re...
Dominant optic atrophy (DOA) is an inherited mitochondrial disease leading to specific degeneration ...
Autosomal dominant optic atrophy (ADOA), the commonest cause of inherited optic atrophy, is caused b...
Optic atrophy (OA) with autosomal inheritance is a form of optic neuropathy characterized by the pro...
Autosomal dominant optic atrophy (ADOA) is a slowly progressive ocular disorder associated with reti...
Purpose: Retinal ganglion cells (RGCs) are susceptible to mitochondrial deficits and also the major ...
none13noneLODI R; TONON C; VALENTINO ML; IOTTI S; CLEMENTI V; MALUCELLI E; BARBONI P; LONGANESI L; S...
Autosomal Dominant Optic Atrophy (ADOA) is the most common inherited optic atrophy where vision impa...
Mutations in the OPA1 gene product result in the most common form of autosomal dominant optic atroph...
none13noneZanna C.; Ghelli A.; Porcelli A.M.; Karbowski M.; Youle R.J.; Schimpf S.; Wissinger B.; Pi...
Autosomal dominant optic atrophy (ADOA) is a progressive ophthalmologic disorder caused in two-third...
The aim of this study was to determine the pathogenetic mechanism of autosomal dominant optic atroph...
To characterize the molecular links between type-1 autosomal dominant optic atrophy (ADOA) and OPA1 ...
International audienceThe OPA1 gene, encoding a dynamin-like mitochondrial GTPase, is involved in au...
Autosomal dominant optic atrophy (ADOA), the commonest cause of inherited optic atrophy, is caused b...
AbstractAutosomal Dominant Optic Atrophy (ADOA) is characterized by the selective degeneration of re...
Dominant optic atrophy (DOA) is an inherited mitochondrial disease leading to specific degeneration ...
Autosomal dominant optic atrophy (ADOA), the commonest cause of inherited optic atrophy, is caused b...
Optic atrophy (OA) with autosomal inheritance is a form of optic neuropathy characterized by the pro...
Autosomal dominant optic atrophy (ADOA) is a slowly progressive ocular disorder associated with reti...
Purpose: Retinal ganglion cells (RGCs) are susceptible to mitochondrial deficits and also the major ...