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Q27027853-B6E7970D-DBCD-425F-A319-8D8D6D617A12
Q27027853-B6E7970D-DBCD-425F-A319-8D8D6D617A12
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27027853-B6E7970D-DBCD-425F-A319-8D8D6D617A12
Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs
P2860
Q27027853-B6E7970D-DBCD-425F-A319-8D8D6D617A12
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27027853-B6E7970D-DBCD-425F-A319-8D8D6D617A12
rank
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type
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Statement
wasDerivedFrom
98005e5074460e7a71d17a98528cc9d728721f12
P2860
A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).