Further evidence for genetic heterogeneity of autosomal dominant disorders with accumulation of multiple deletions of mitochondrial DNA

[...]different modes of inheritance are encountered in disorders of oxidative phosphorylation.

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of medical genetics 2000-07, Vol.37 (7), p.547-548
Hauptverfasser:	VAN GOETHEM, GERT, LÖFGREN, ANN, MARTIN, JEAN-JACQUES, VAN BROECKHOVEN, CHRISTINE
Format:	Artikel
Sprache:	eng
Schlagworte:	Biopsy Chromosome Aberrations - genetics Chromosome Disorders Chromosomes Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 4 Computer simulation Defects Deoxyribonucleic acid DNA DNA, Mitochondrial - blood DNA, Mitochondrial - genetics Female Gene Deletion Genes Genes, Dominant - genetics Genomes Humans Letters to the Editor Lod Score Male Mitochondrial DNA Mutation Ophthalmoplegia, Chronic Progressive External - genetics Pedigree Phosphorylation
Online-Zugang:	Volltext
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Beschreibung
Zusammenfassung:	[...]different modes of inheritance are encountered in disorders of oxidative phosphorylation.
ISSN:	0022-2593 1468-6244 1468-6244
DOI:	10.1136/jmg.37.7.547