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Q34839861-BDF16B0A-6482-46D2-88EB-C1B3E2BEA614
Q34839861-BDF16B0A-6482-46D2-88EB-C1B3E2BEA614
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http://www.wikidata.org/entity/statement/Q34839861-BDF16B0A-6482-46D2-88EB-C1B3E2BEA614
Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus.
P2860
Q34839861-BDF16B0A-6482-46D2-88EB-C1B3E2BEA614
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34839861-BDF16B0A-6482-46D2-88EB-C1B3E2BEA614
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wasDerivedFrom
d629f3f3961c02fda61117edc17ade38d4dcb61a
P2860
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.