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Q28078294-F30DCD60-0F93-4381-9CAD-7CEEC05A6B01
Q28078294-F30DCD60-0F93-4381-9CAD-7CEEC05A6B01
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http://www.wikidata.org/entity/statement/Q28078294-F30DCD60-0F93-4381-9CAD-7CEEC05A6B01
The neurobiology of the Prader-Willi phenotype of fragile X syndrome
P2860
Q28078294-F30DCD60-0F93-4381-9CAD-7CEEC05A6B01
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http://www.wikidata.org/entity/statement/Q28078294-F30DCD60-0F93-4381-9CAD-7CEEC05A6B01
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wasDerivedFrom
c1d30a8fb3bd53be3e58e1086c0b8db5c14706e3
P2860
Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.