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Q37092297-3B1E8EA0-DE92-4F5F-A293-128A91016FF4
Q37092297-3B1E8EA0-DE92-4F5F-A293-128A91016FF4
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http://www.wikidata.org/entity/statement/Q37092297-3B1E8EA0-DE92-4F5F-A293-128A91016FF4
Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.
P2860
Q37092297-3B1E8EA0-DE92-4F5F-A293-128A91016FF4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37092297-3B1E8EA0-DE92-4F5F-A293-128A91016FF4
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wasDerivedFrom
c6ad1a90202431af6250cea450d5f15a21131802
P2860
Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.