(Q40678892)
Statements
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Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G). (English)
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Pastores GM
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Santorelli FM
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Shanske S
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Gelb BD
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Fyfe B
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Wolfe D
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Willner JP
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1 April 1994
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50
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3
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265-271
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Identifiers
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