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Q41438555-AF2B6631-12D7-48D2-92DA-ED4C2EFBC1C7
Q41438555-AF2B6631-12D7-48D2-92DA-ED4C2EFBC1C7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41438555-AF2B6631-12D7-48D2-92DA-ED4C2EFBC1C7
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant mice.
P2860
Q41438555-AF2B6631-12D7-48D2-92DA-ED4C2EFBC1C7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41438555-AF2B6631-12D7-48D2-92DA-ED4C2EFBC1C7
rank
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type
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Statement
wasDerivedFrom
11c191332f5597f9f345cd745d9d60babe07009a
P2860
Mutations in KCTD1 cause scalp-ear-nipple syndrome.