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Q35272233-3299CEB3-C769-4978-8673-239FB2B15382
Q35272233-3299CEB3-C769-4978-8673-239FB2B15382
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35272233-3299CEB3-C769-4978-8673-239FB2B15382
Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria.
P2860
Q35272233-3299CEB3-C769-4978-8673-239FB2B15382
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35272233-3299CEB3-C769-4978-8673-239FB2B15382
rank
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type
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Statement
wasDerivedFrom
9d18a6ca8674aaccef90e91b84a4c2d82a7b8cdc
P2860
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East.