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Q33821565-F0F62100-2EFE-4373-A279-2DA0B4971DD2
Q33821565-F0F62100-2EFE-4373-A279-2DA0B4971DD2
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Statement
http://www.wikidata.org/entity/statement/Q33821565-F0F62100-2EFE-4373-A279-2DA0B4971DD2
Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease.
P2860
Q33821565-F0F62100-2EFE-4373-A279-2DA0B4971DD2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33821565-F0F62100-2EFE-4373-A279-2DA0B4971DD2
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wasDerivedFrom
6bfd10978e0198d02e969c1ec63befc11efd31ca
P2860
A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).