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Q48300271-0655E2B1-2FA6-4F7F-A6AE-7C0A2AE68464
Q48300271-0655E2B1-2FA6-4F7F-A6AE-7C0A2AE68464
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Statement
http://www.wikidata.org/entity/statement/Q48300271-0655E2B1-2FA6-4F7F-A6AE-7C0A2AE68464
FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome.
P2860
Q48300271-0655E2B1-2FA6-4F7F-A6AE-7C0A2AE68464
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48300271-0655E2B1-2FA6-4F7F-A6AE-7C0A2AE68464
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wasDerivedFrom
13e7f8d8d7c46d7a0df6d66e2777e68532688acc
P2860
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.