none13noneZanna C.; Ghelli A.; Porcelli A.M.; Karbowski M.; Youle R.J.; Schimpf S.; Wissinger B.; Pinti M.; Cossarizza A.; Vidoni S.; Valentino M.L.; Rugolo M.; Carelli V.Zanna C.; Ghelli A.; Porcelli A.M.; Karbowski M.; Youle R.J.; Schimpf S.; Wissinger B.; Pinti M.; Cossarizza A.; Vidoni S.; Valentino M.L.; Rugolo M.; Carelli V
International audienceDominant optic atrophy (DOA) is an inherited mitochondrial disease leading to ...
Abstract Background Heterozygous mutations in OPA1 are a common cause of autosomal dominant optic at...
Autosomal dominant optic atrophy (ADOA) is a progressive ophthalmologic disorder caused in two-third...
none12noneC. Tonon; R. Lodi; D. N. Manners; E. Malucelli; C. Testa; M. L. Valentino; P. Barboni; S. ...
none14noneBarboni P.; Carbonelli M.; Savini G.; Foscarini B.; Parisi V.; Valentino M.L.; Carta A.; D...
none13noneLODI R; TONON C; VALENTINO ML; IOTTI S; CLEMENTI V; MALUCELLI E; BARBONI P; LONGANESI L; S...
none25Dominant optic atrophy (DOA) is genetically heterogeneous and pathogenic mutations have been i...
To investigate mitophagy in 5 patients with severe dominantly inherited optic atrophy (DOA), caused ...
Mutations in the OPA1 gene product result in the most common form of autosomal dominant optic atroph...
Autosomal Dominant Optic Atrophy (ADOA) is the most common inherited optic atrophy where vision impa...
none34Mutations in OPA1, a dynamin-related GTPase involved in mitochondrial fusion, cristae organiza...
AbstractAutosomal Dominant Optic Atrophy (ADOA) is characterized by the selective degeneration of re...
To characterize the molecular links between type-1 autosomal dominant optic atrophy (ADOA) and OPA1 ...
Dominant optic atrophy (DOA) is characterized by retinal ganglion cell degeneration leading to optic...
Dominant optic atrophy (DOA) is an inherited mitochondrial disease leading to specific degeneration ...
International audienceDominant optic atrophy (DOA) is an inherited mitochondrial disease leading to ...
Abstract Background Heterozygous mutations in OPA1 are a common cause of autosomal dominant optic at...
Autosomal dominant optic atrophy (ADOA) is a progressive ophthalmologic disorder caused in two-third...
none12noneC. Tonon; R. Lodi; D. N. Manners; E. Malucelli; C. Testa; M. L. Valentino; P. Barboni; S. ...
none14noneBarboni P.; Carbonelli M.; Savini G.; Foscarini B.; Parisi V.; Valentino M.L.; Carta A.; D...
none13noneLODI R; TONON C; VALENTINO ML; IOTTI S; CLEMENTI V; MALUCELLI E; BARBONI P; LONGANESI L; S...
none25Dominant optic atrophy (DOA) is genetically heterogeneous and pathogenic mutations have been i...
To investigate mitophagy in 5 patients with severe dominantly inherited optic atrophy (DOA), caused ...
Mutations in the OPA1 gene product result in the most common form of autosomal dominant optic atroph...
Autosomal Dominant Optic Atrophy (ADOA) is the most common inherited optic atrophy where vision impa...
none34Mutations in OPA1, a dynamin-related GTPase involved in mitochondrial fusion, cristae organiza...
AbstractAutosomal Dominant Optic Atrophy (ADOA) is characterized by the selective degeneration of re...
To characterize the molecular links between type-1 autosomal dominant optic atrophy (ADOA) and OPA1 ...
Dominant optic atrophy (DOA) is characterized by retinal ganglion cell degeneration leading to optic...
Dominant optic atrophy (DOA) is an inherited mitochondrial disease leading to specific degeneration ...
International audienceDominant optic atrophy (DOA) is an inherited mitochondrial disease leading to ...
Abstract Background Heterozygous mutations in OPA1 are a common cause of autosomal dominant optic at...
Autosomal dominant optic atrophy (ADOA) is a progressive ophthalmologic disorder caused in two-third...
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