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Q37802413-3EDE6FB0-3F84-4631-BF3C-0154B0746931
Q37802413-3EDE6FB0-3F84-4631-BF3C-0154B0746931
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37802413-3EDE6FB0-3F84-4631-BF3C-0154B0746931
Hereditary kidney diseases: highlighting the importance of classical Mendelian phenotypes.
P2860
Q37802413-3EDE6FB0-3F84-4631-BF3C-0154B0746931
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37802413-3EDE6FB0-3F84-4631-BF3C-0154B0746931
rank
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Statement
wasDerivedFrom
41ccdf420a31d7fd3e04ce1339082cab505ce221
P2860
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations