Electrocardiographic abnormalities in Leber's hereditary optic atrophy
- 1 June 1987
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 10 (S2) , 256-259
- https://doi.org/10.1007/bf01811419
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Deficiency of thiosulphate sulphurtransferase (rhodanese) in Leber's hereditary optic neuropathy.BMJ, 1986
- PRE-EXCITATION SYNDROME AND LEBER'S HEREDITARY OPTIC NEURORETINOPATHYThe Lancet, 1985
- New aspects of the genetic, etiologic, and clinical puzzle of Leber's diseaseNeurology, 1984
- Decreased thiosulfate sulfur transferase (rhodanese) in Leber's hereditary optic atrophyJournal of Molecular Medicine, 1984
- The heart in Leber's optic atrophy.British Journal of Ophthalmology, 1970
- LEBER’S HEREDITARY OPTIC ATROPHY SOME CLINICAL AND AETIOLOGICAL CONSIDERATIONSBrain, 1963
- A CLINICAL STUDY OF AN HEREDO-FAMILIAL DISEASE RESEMBLING DISSEMINATED SCLEROSISBrain, 1929