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Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy

✍ Scribed by S. Bannwarth; V. Procaccio; C. Rouzier; K. Fragaki; J. Poole; B. Chabrol; C. Desnuelle; J. Pouget; J.P. Azulay; S. Attarian; J.F. Pellissier; J.J. Gargus; J.E. Abdenur; T. Mozaffar; P. Calvas; P. Labauge; M. Pages; D.C. Wallace; J.C. Lambert; V. Paquis-Flucklinger


Book ID
116751766
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
174 KB
Volume
8
Category
Article
ISSN
1567-7249

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Molecular analysis of mitochondrial DNA (mtDNA) is a critical step in diagnosis and genetic counseling of respiratory chain defects. No fast method is currently available for the identification of unknown mtDNA point mutations. We have developed a new strategy based on complete mtDNA PCR amplificati