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Q36811500-191E3F29-D9E7-4A2E-A15E-B3390038DFA1
Q36811500-191E3F29-D9E7-4A2E-A15E-B3390038DFA1
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Statement
http://www.wikidata.org/entity/statement/Q36811500-191E3F29-D9E7-4A2E-A15E-B3390038DFA1
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
Q36811500-191E3F29-D9E7-4A2E-A15E-B3390038DFA1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36811500-191E3F29-D9E7-4A2E-A15E-B3390038DFA1
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wasDerivedFrom
e11a014104fcd60e522307860cf4dc83322acba7
P2860
Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation