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Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia

✍ Scribed by SafarinaG. Malik; Nova Pieter; Herawati Sudoyo; Abdul Kadir; Sangkot Marzuki


Publisher
Nature Publishing Group
Year
2003
Tongue
English
Weight
216 KB
Volume
48
Category
Article
ISSN
1435-232X

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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