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Q33793717-953DE0A4-8500-4A3C-BA85-907F720DCC3B
Q33793717-953DE0A4-8500-4A3C-BA85-907F720DCC3B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33793717-953DE0A4-8500-4A3C-BA85-907F720DCC3B
Mitochondrial disorders. A diagnostic challenge in clinical chemistry.
P2860
Q33793717-953DE0A4-8500-4A3C-BA85-907F720DCC3B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33793717-953DE0A4-8500-4A3C-BA85-907F720DCC3B
rank
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Statement
wasDerivedFrom
ad0f3cb3039eaf684598d7bed66de5d95bbc4078
P2860
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter