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10. An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA). Helmken C; Wetter A; Rudnik-Schöneborn S; Liehr T; Zerres K; Wirth B Eur J Hum Genet; 2000 Jul; 8(7):493-9. PubMed ID: 10909848 [TBL] [Abstract][Full Text] [Related]
11. Fibration, fibrillation, and fasciculation: say what you see. van Baalen A; Stephani U Clin Neurophysiol; 2007 Jun; 118(6):1418-20. PubMed ID: 17452004 [No Abstract] [Full Text] [Related]
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14. Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature. Haliloglu G; Chattopadhyay A; Skorodis L; Manzur A; Mercuri E; Talim B; Akçören Z; Renda Y; Muntoni F; Topaloğlu H Neuropediatrics; 2002 Dec; 33(6):314-9. PubMed ID: 12571787 [TBL] [Abstract][Full Text] [Related]
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17. Clinical and molecular genetic features of congenital spinal muscular atrophy. Devriendt K; Lammens M; Schollen E; Van Hole C; Dom R; Devlieger H; Cassiman JJ; Fryns JP; Matthijs G Ann Neurol; 1996 Nov; 40(5):731-8. PubMed ID: 8957014 [TBL] [Abstract][Full Text] [Related]
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19. Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy. Ben Hamida C; Soussi-Yanicostas N; Butler-Browne GS; Bejaoui K; Hentati F; Ben Hamida M Muscle Nerve; 1994 Apr; 17(4):400-10. PubMed ID: 8170486 [TBL] [Abstract][Full Text] [Related]
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