0392766 - ÚOCHB 2014 RIV DK eng J - Journal Article
Lisková, P. - Ulmanová, O. - Těšina, Petr - Melsová, H. - Diblik, P. - Hansíková, H. - Tesařová, M. - Votruba, M.
Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder.
Acta Ophthalmologica. Roč. 91, č. 3 (2013), E225-E231. ISSN 1755-375X. E-ISSN 1755-3768
Grant - others:GA MZd(CZ) NT11190
Institutional research plan: CEZ:AV0Z40550506
Keywords : ataxia * autosomal dominant * deafness * encephalomyopathy
Subject RIV: FF - HEENT, Dentistry
Impact factor: 2.512, year: 2013
Permanent Link: http://hdl.handle.net/11104/0221562
Lisková, P. - Ulmanová, O. - Těšina, Petr - Melsová, H. - Diblik, P. - Hansíková, H. - Tesařová, M. - Votruba, M.
Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder.
Acta Ophthalmologica. Roč. 91, č. 3 (2013), E225-E231. ISSN 1755-375X. E-ISSN 1755-3768
Grant - others:GA MZd(CZ) NT11190
Institutional research plan: CEZ:AV0Z40550506
Keywords : ataxia * autosomal dominant * deafness * encephalomyopathy
Subject RIV: FF - HEENT, Dentistry
Impact factor: 2.512, year: 2013
Permanent Link: http://hdl.handle.net/11104/0221562