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PRRT2-Associated Paroxysmal Movement Disorders.
2018 Jan 11. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
2018 Jan 11. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID: 29334453
Free Books & Documents.
Review.
The evolving spectrum of PRRT2-associated paroxysmal diseases.
Ebrahimi-Fakhari D, Saffari A, Westenberger A, Klein C.
Ebrahimi-Fakhari D, et al.
Brain. 2015 Dec;138(Pt 12):3476-95. doi: 10.1093/brain/awv317. Epub 2015 Nov 23.
Brain. 2015.
PMID: 26598493
Review.
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Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis.
Yang X, Zhang Y, Xu X, Wang S, Yang Z, Wu Y, Liu X, Wu X.
Yang X, et al.
BMC Neurol. 2013 Dec 26;13:209. doi: 10.1186/1471-2377-13-209.
BMC Neurol. 2013.
PMID: 24370076
Free PMC article.
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