Mitochondrial mutations of Leber's hereditary optic neuropathy : a risk factor for multiple sclerosis

Multiple sclerosis (MS) and Leber's hereditary optic neuropathy (LHON) have been found to occur in combination. Based on an extensive literature search and on a clinical analysis of 55 LHON pedigrees (103 patients) and 40 patients with definite MS, this study concludes that the association of L...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Journal of neurology 2000-07, Vol.247 (7), p.535-543
Hauptverfasser:	VANOPDENBOSCH, L, DUBOIS, B, D'HOOGHE, M.-B, MEIRE, F, CARTON, H
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Aged Ataxia Atrophy Biological and medical sciences Diseases of visual field, optic nerve, optic chiasma and optic tracts DNA Mutational Analysis DNA, Mitochondrial - genetics Female Genetic Testing Humans Male Medical sciences Middle Aged Mitochondrial DNA Multiple sclerosis Multiple Sclerosis - etiology Multiple Sclerosis - genetics Mutation Neurology Ophthalmology Optic Atrophies, Hereditary - complications Optic Atrophies, Hereditary - genetics Paresis Pedigree Risk Factors Severity of Illness Index
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!