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Q38970382-511875B5-F582-4AAF-9920-84D954E74E99
Q38970382-511875B5-F582-4AAF-9920-84D954E74E99
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38970382-511875B5-F582-4AAF-9920-84D954E74E99
Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1.
P2860
Q38970382-511875B5-F582-4AAF-9920-84D954E74E99
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38970382-511875B5-F582-4AAF-9920-84D954E74E99
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type
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wasDerivedFrom
cb817794123c7770f6c2ee78acd623f9d465ad93
P2860
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy