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2
Q41330979-99DEFB48-07AF-4768-8A55-8DC6FEE6703A
Q41330979-99DEFB48-07AF-4768-8A55-8DC6FEE6703A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41330979-99DEFB48-07AF-4768-8A55-8DC6FEE6703A
Novel AMPD2 mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalities.
P2860
Q41330979-99DEFB48-07AF-4768-8A55-8DC6FEE6703A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41330979-99DEFB48-07AF-4768-8A55-8DC6FEE6703A
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type
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Statement
wasDerivedFrom
3fe646bbd99cef07af17bb3b0d2e604530163a99
P2860
A mutation in Ampd2 is associated with nephrotic syndrome and hypercholesterolemia in mice