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The Mitochondrial DNA A3243A>G Mutation Must Be An Infrequent Cause Of Asperger Syndrome

✍ Scribed by Lindsey Kent; Claire Lambert; Angela Pyle; Hannah Elliott; Sally Wheelwright; Simon Baron-Cohen; Patrick F. Chinnery


Book ID
116683616
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
199 KB
Volume
149
Category
Article
ISSN
1097-6833

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Prevalence, segregation, and phenotype o
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## Abstract ## Objective We studied the prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children in a defined population in Northern Ostrobothnia, Finland. ## Methods Children with diagnoses commonly associated with mitochondrial diseases were ascertained. Blo