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9. Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes. Tezenas du Montcel S; Clot F; Vidailhet M; Roze E; Damier P; Jedynak CP; Camuzat A; Lagueny A; Vercueil L; Doummar D; Guyant-Maréchal L; Houeto JL; Ponsot G; Thobois S; Cournelle MA; Durr A; Durif F; Echenne B; Hannequin D; Tranchant C; Brice A; J Med Genet; 2006 May; 43(5):394-400. PubMed ID: 16227522 [TBL] [Abstract][Full Text] [Related]
10. Phenotypic features of myoclonus-dystonia in three kindreds. Doheny DO; Brin MF; Morrison CE; Smith CJ; Walker RH; Abbasi S; Müller B; Garrels J; Liu L; De Carvalho Aguiar P; Schilling K; Kramer P; De Leon D; Raymond D; Saunders-Pullman R; Klein C; Bressman SB; Schmand B; Tijssen MA; Ozelius LJ; Silverman JM Neurology; 2002 Oct; 59(8):1187-96. PubMed ID: 12391346 [TBL] [Abstract][Full Text] [Related]
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12. A novel GNAL mutation in familial dystonia presenting with childhood tremor and myoclonus. Geoghegan AR; Al Hussona M; Beauchamp NJ; Hutchinson M; Sean O'Riordan MB; Lynch T; Webb D Mov Disord; 2019 Jun; 34(6):923-924. PubMed ID: 30964956 [No Abstract] [Full Text] [Related]
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14. Mutations in the epsilon-sarcoglycan gene found to be uncommon in seven myoclonus-dystonia families. Han F; Lang AE; Racacho L; Bulman DE; Grimes DA Neurology; 2003 Jul; 61(2):244-6. PubMed ID: 12874409 [TBL] [Abstract][Full Text] [Related]
15. A neurophysiological study of myoclonus in patients with DYT11 myoclonus-dystonia syndrome. Marelli C; Canafoglia L; Zibordi F; Ciano C; Visani E; Zorzi G; Garavaglia B; Barzaghi C; Albanese A; Soliveri P; Leone M; Panzica F; Scaioli V; Pincherle A; Nardocci N; Franceschetti S Mov Disord; 2008 Oct; 23(14):2041-8. PubMed ID: 18759336 [TBL] [Abstract][Full Text] [Related]
16. Distal myoclonus and late onset in a large Dutch family with myoclonus-dystonia. Foncke EM; Gerrits MC; van Ruissen F; Baas F; Hedrich K; Tijssen CC; Klein C; Tijssen MA Neurology; 2006 Nov; 67(9):1677-80. PubMed ID: 17101905 [TBL] [Abstract][Full Text] [Related]
17. Myoclonus-dystonia: detection of novel, recurrent, and de novo SGCE mutations. Hedrich K; Meyer EM; Schüle B; Kock N; de Carvalho Aguiar P; Wiegers K; Koelman JH; Garrels J; Dürr R; Liu L; Schwinger E; Ozelius LJ; Landwehrmeyer B; Stoessl AJ; Tijssen MA; Klein C Neurology; 2004 Apr; 62(7):1229-31. PubMed ID: 15079037 [No Abstract] [Full Text] [Related]
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20. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Zimprich A; Grabowski M; Asmus F; Naumann M; Berg D; Bertram M; Scheidtmann K; Kern P; Winkelmann J; Müller-Myhsok B; Riedel L; Bauer M; Müller T; Castro M; Meitinger T; Strom TM; Gasser T Nat Genet; 2001 Sep; 29(1):66-9. PubMed ID: 11528394 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]