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Q24310789-93230AEF-1FCD-40E3-A8ED-60FEB0F37706
Q24310789-93230AEF-1FCD-40E3-A8ED-60FEB0F37706
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Statement
http://www.wikidata.org/entity/statement/Q24310789-93230AEF-1FCD-40E3-A8ED-60FEB0F37706
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome
P2860
Q24310789-93230AEF-1FCD-40E3-A8ED-60FEB0F37706
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24310789-93230AEF-1FCD-40E3-A8ED-60FEB0F37706
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wasDerivedFrom
fe1e63f543ba9336189dc692aa54231507fc0e07
P2860
Evidence that the peptidylprolyl isomerase domain of the hsp90-binding immunophilin FKBP52 is involved in both dynein interaction and glucocorticoid receptor movement to the nucleus