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Q36811500-ABDDE74A-4E17-4600-AD22-8795840D5356
Q36811500-ABDDE74A-4E17-4600-AD22-8795840D5356
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36811500-ABDDE74A-4E17-4600-AD22-8795840D5356
Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.
P2860
Q36811500-ABDDE74A-4E17-4600-AD22-8795840D5356
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36811500-ABDDE74A-4E17-4600-AD22-8795840D5356
rank
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type
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wasDerivedFrom
e11a014104fcd60e522307860cf4dc83322acba7
P2860
Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation