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Q42605402-0CA6A56B-4C5E-4040-9649-0D02B6E9D8F2
Q42605402-0CA6A56B-4C5E-4040-9649-0D02B6E9D8F2
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http://www.wikidata.org/entity/statement/Q42605402-0CA6A56B-4C5E-4040-9649-0D02B6E9D8F2
Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome.
P2860
Q42605402-0CA6A56B-4C5E-4040-9649-0D02B6E9D8F2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42605402-0CA6A56B-4C5E-4040-9649-0D02B6E9D8F2
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wasDerivedFrom
640c2134157a402290b3d98e9badf53d990bcdf8
P2860
Structure and function correlations at the imprinted mouse Snrpn locus.