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Q36277419-2961FC17-0DF9-41CA-97CF-56AFCEA3AF79
Q36277419-2961FC17-0DF9-41CA-97CF-56AFCEA3AF79
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36277419-2961FC17-0DF9-41CA-97CF-56AFCEA3AF79
A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease.
P2860
Q36277419-2961FC17-0DF9-41CA-97CF-56AFCEA3AF79
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36277419-2961FC17-0DF9-41CA-97CF-56AFCEA3AF79
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wasDerivedFrom
b04272e9c9dce7babc285484bdfe889c783088e2
P2860
Complete mitochondrial DNA sequence analysis in two southern Chinese pedigrees with Leber hereditary optic neuropathy revealed secondary mutations along with the primary mutation.