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Q39381468-77B3339A-79D3-450D-AF38-F882065E20C8
Q39381468-77B3339A-79D3-450D-AF38-F882065E20C8
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http://www.wikidata.org/entity/statement/Q39381468-77B3339A-79D3-450D-AF38-F882065E20C8
Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.
P2860
Q39381468-77B3339A-79D3-450D-AF38-F882065E20C8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39381468-77B3339A-79D3-450D-AF38-F882065E20C8
rank
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Statement
wasDerivedFrom
dfe34550119b651dd39e816fa7216a66557ea454
P2860
Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis.