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Q36062909-3F7C1F7C-5865-4F1B-BC07-BED31D821918
Q36062909-3F7C1F7C-5865-4F1B-BC07-BED31D821918
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http://www.wikidata.org/entity/statement/Q36062909-3F7C1F7C-5865-4F1B-BC07-BED31D821918
Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report
P2860
Q36062909-3F7C1F7C-5865-4F1B-BC07-BED31D821918
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36062909-3F7C1F7C-5865-4F1B-BC07-BED31D821918
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wasDerivedFrom
e33b0b460f1250be7197e21b2b69095191b26c91
P2860
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome