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Q28271033-33471F6E-44C1-416A-A139-5AB9CF613801
Q28271033-33471F6E-44C1-416A-A139-5AB9CF613801
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http://www.wikidata.org/entity/statement/Q28271033-33471F6E-44C1-416A-A139-5AB9CF613801
A mouse model for Prader-Willi syndrome imprinting-centre mutations
P2860
Q28271033-33471F6E-44C1-416A-A139-5AB9CF613801
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28271033-33471F6E-44C1-416A-A139-5AB9CF613801
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wasDerivedFrom
4cac8a6e9247537a9bf68d44ef9a54f83733ba1c
P2860
The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse