Screening for mitochondrial DNA heteroplasmy in children at risk for mitochondrial disease
- 30 September 2001
- journal article
- Published by Elsevier in Mitochondrion
- Vol. 1 (3) , 269-278
- https://doi.org/10.1016/s1567-7249(01)00028-9
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Persistent Heteroplasmy of a Mutation in the Human mtDNA Control Region: Hypermutation as an Apparent Consequence of Simple-Repeat Expansion/ContractionAmerican Journal of Human Genetics, 2000
- The Frequency of Heteroplasmy in the HVII Region of mtDNA Differs across Tissue Types and Increases with AgeAmerican Journal of Human Genetics, 2000
- Identification in Portugal and Brazil of a mtDNA Lineage Containing a 9-bp Triplication of the Intergenic COII/tRNALys RegionHuman Heredity, 1999
- Heteroplasmic substitutions in the mitochondrial DNA control region in mother and child samples.International journal of legal medicine, 1998
- Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison diseaseEuropean Journal of Pediatrics, 1998
- Transmission of mitochondrial DNA heteroplasmy in normal pedigreesHuman Genetics, 1998
- Slowly but surely towards better scanning for mutationsTrends in Genetics, 1997
- Mitochondrial DNA sequence heteroplasmy in the Grand Duke of Russia Georgij Romanov establishes the authenticity of the remains of Tsar Nicholas IINature Genetics, 1996
- Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafnessPharmacogenetics, 1995
- Mitochondrial gene segregation in mammals: is the bottleneck always narrow?Human Genetics, 1992