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Q28189572-891DBED1-7BF6-4C19-B293-E25E1662958B
Q28189572-891DBED1-7BF6-4C19-B293-E25E1662958B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28189572-891DBED1-7BF6-4C19-B293-E25E1662958B
Respiratory chain complex I deficiency
P2860
Q28189572-891DBED1-7BF6-4C19-B293-E25E1662958B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28189572-891DBED1-7BF6-4C19-B293-E25E1662958B
rank
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type
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wasDerivedFrom
7be63a3840d56584a2a5392950719d8f75aaa1c2
P2860
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNA.