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Q47922275-871C945A-C267-4363-A162-97832735C415
Q47922275-871C945A-C267-4363-A162-97832735C415
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http://www.wikidata.org/entity/statement/Q47922275-871C945A-C267-4363-A162-97832735C415
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions.
P2860
Q47922275-871C945A-C267-4363-A162-97832735C415
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47922275-871C945A-C267-4363-A162-97832735C415
rank
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type
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wasDerivedFrom
883473f7bd62c6902262be49384d65d16d95caf6
P2860
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.