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Q28235995-5316A83B-318A-4317-9C95-0559B6288B63
Q28235995-5316A83B-318A-4317-9C95-0559B6288B63
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235995-5316A83B-318A-4317-9C95-0559B6288B63
A loss-of-function mutation in natriuretic peptide receptor 2 (Npr2) gene is responsible for disproportionate dwarfism in cn/cn mouse
P2860
Q28235995-5316A83B-318A-4317-9C95-0559B6288B63
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235995-5316A83B-318A-4317-9C95-0559B6288B63
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7f6cdccccc46c36def048f5757ee5b6a264c24c2
P2860
Receptor selectivity of natriuretic peptide family, atrial natriuretic peptide, brain natriuretic peptide, and C-type natriuretic peptide