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Detection of Common Disease-Causing Mutations in Mitochondrial DNA (Mitochondrial Encephalomyopathy, Lactic Acidosis with Stroke-Like Episodes MTTL1 3243 A>G and Myoclonic Epilepsy Associated with Ragged-Red Fibers MTTK 8344A>G) by Real-Time Polymerase Chain Reaction

✍ Scribed by Fan, Hongxin; Civalier, Chris; Booker, Jessica K.; Gulley, Margaret L.; Prior, Thomas W.; Farber, Rosann A.


Book ID
121427342
Publisher
American Society for Investigative Pathology
Year
2006
Tongue
English
Weight
369 KB
Volume
8
Category
Article
ISSN
1525-1578

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