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New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndrome..
Arch Neurol
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Pelka, GJ, Watson, CM, Christodoulou, J, Tam, PPL.
Distinct expression profiles of Mecp2 transcripts with different lengths of 3'UTR in the brain and visceral organs during mouse development..
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2005
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Biggin, A, Henke, R, Bennetts, B, Thorburn, DR, Christodoulou, J.
Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography..
Mol Genet Metab
84(1)
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2005
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Moore, H, Leonard, H, de Klerk, N, Robertson, I, Fyfe, S, Christodoulou, J, Weaving, L, Davis, M, Mulroy, S, Colvin, L.
Health service use in Rett syndrome..
J Child Neurol
20(1)
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2005
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Neas, K, Bennetts, B, Carpenter, K, White, R, Kirk, EP, Wilson, M, Kelley, R, Baric, I, Christodoulou, J.
OPA3 mutation screening in patients with unexplained 3-methylglutaconic aciduria..
J Inherit Metab Dis
28(4)
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