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Human Genetics|September 1, 1995
De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspringM H Tulinius, M Houshmand, N G Larsson, et al.
European Journal of Pediatrics|January 1, 1995
Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletionsM H Tulinius, A Oldfors, E Holme, et al.
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