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2. A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197. Auburger G, Ratzlaff T, Lunkes A, Nelles HW, Leube B, Binkofski F, Kugel H, Heindel W, Seitz R, Benecke R, Witte OW, Voit T. Genomics; 1996 Jan 01; 31(1):90-4. PubMed ID: 8808284 [Abstract] [Full Text] [Related]
9. Chorea as a manifestation of familial paroxysmal choreoathetosis. Horner FA, Jackson L. Neurology; 1968 Mar 01; 18(3):277. PubMed ID: 5689676 [No Abstract] [Full Text] [Related]
10. Idiopathic hypoparathyroidism and paroxysmal kinesigenic choreoathetosis. Micheli F, Pardal MF, Parera IC, Giannaula R. Ann Neurol; 1989 Sep 01; 26(3):415. PubMed ID: 2802542 [No Abstract] [Full Text] [Related]
11. Paroxysmal kinesigenic choreoathetosis: from first discovery in 1892 to genetic linkage with benign familial infantile convulsions. Kato N, Sadamatsu M, Kikuchi T, Niikawa N, Fukuyama Y. Epilepsy Res; 2006 Aug 01; 70 Suppl 1():S174-84. PubMed ID: 16901678 [Abstract] [Full Text] [Related]