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Q28235995-43C737BF-0BC7-48FC-8B98-B28D79E44B02
Q28235995-43C737BF-0BC7-48FC-8B98-B28D79E44B02
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235995-43C737BF-0BC7-48FC-8B98-B28D79E44B02
A loss-of-function mutation in natriuretic peptide receptor 2 (Npr2) gene is responsible for disproportionate dwarfism in cn/cn mouse
P2860
Q28235995-43C737BF-0BC7-48FC-8B98-B28D79E44B02
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235995-43C737BF-0BC7-48FC-8B98-B28D79E44B02
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type
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wasDerivedFrom
7f6cdccccc46c36def048f5757ee5b6a264c24c2
P2860
Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia