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Q37802413-21A546FA-6A63-46B7-A95A-1F1E66DE1CDB
Q37802413-21A546FA-6A63-46B7-A95A-1F1E66DE1CDB
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http://www.wikidata.org/entity/statement/Q37802413-21A546FA-6A63-46B7-A95A-1F1E66DE1CDB
Hereditary kidney diseases: highlighting the importance of classical Mendelian phenotypes.
P2860
Q37802413-21A546FA-6A63-46B7-A95A-1F1E66DE1CDB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37802413-21A546FA-6A63-46B7-A95A-1F1E66DE1CDB
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wasDerivedFrom
41ccdf420a31d7fd3e04ce1339082cab505ce221
P2860
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis