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Q47706180-05A43533-0481-4862-8478-4B7DB667B0CB
Q47706180-05A43533-0481-4862-8478-4B7DB667B0CB
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Statement
http://www.wikidata.org/entity/statement/Q47706180-05A43533-0481-4862-8478-4B7DB667B0CB
The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways.
P2860
Q47706180-05A43533-0481-4862-8478-4B7DB667B0CB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47706180-05A43533-0481-4862-8478-4B7DB667B0CB
rank
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type
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Statement
wasDerivedFrom
f50ca6cf4ff3e5702ec2942291d5ba6a2f3d07ad
P2860
Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis.