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Q38187116-FD29A277-7309-42E8-A30B-EAF934F4D8BF
Q38187116-FD29A277-7309-42E8-A30B-EAF934F4D8BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38187116-FD29A277-7309-42E8-A30B-EAF934F4D8BF
Renal manifestations of genetic mitochondrial disease.
P2860
Q38187116-FD29A277-7309-42E8-A30B-EAF934F4D8BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38187116-FD29A277-7309-42E8-A30B-EAF934F4D8BF
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
e7a247c294216980da14f3a85443b1f4f6a576c2
P2860
A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency