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- W2912154943 abstract "(The American Journal of Human Genetics 87, 593–603; November 12, 2010) In the first sentence of the third paragraph of the Discussion, Lys5 should have been Leu5. The same error appeared in the third sentence of that same paragraph. These errors appeared in the version of the paper published online October 28 but have been corrected in the version published with the November issue. The authors regret the errors. Prodynorphin Mutations Cause the Neurodegenerative Disorder Spinocerebellar Ataxia Type 23Bakalkin et al.The American Journal of Human GeneticsOctober 28, 2010In BriefSpinocerebellar ataxias (SCAs) are dominantly inherited neurodegenerative disorders characterized by progressive cerebellar ataxia and dysarthria. We have identified missense mutations in prodynorphin (PDYN) that cause SCA23 in four Dutch families displaying progressive gait and limb ataxia. PDYN is the precursor protein for the opioid neuropeptides, α-neoendorphin, and dynorphins A and B (Dyn A and B). Dynorphins regulate pain processing and modulate the rewarding effects of addictive substances. Full-Text PDF Open Archive" @default.
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- W2912154943 date "2010-11-01" @default.
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- W2912154943 title "Prodynorphin Mutations Cause the Neurodegenerative Disorder Spinocerebellar Ataxia Type 23" @default.
- W2912154943 doi "https://doi.org/10.1016/j.ajhg.2010.10.030" @default.
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