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24. Major intra-familial variability in Unverricht-Lundborg disease. Nasri A; Zidi S; Kacem I; Mrabet S; Ben Djebara M; Gargouri A; Leguern E; Gouider R Epileptic Disord; 2022 Feb; 24(1):163-170. PubMed ID: 34787084 [TBL] [Abstract][Full Text] [Related]
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26. Advances in the genetics of progressive myoclonus epilepsy. Delgado-Escueta AV; Ganesh S; Yamakawa K Am J Med Genet; 2001; 106(2):129-38. PubMed ID: 11579433 [TBL] [Abstract][Full Text] [Related]
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29. Coexistence of Unverricht-Lundborg disease and congenital deafness: molecular resolution of a complex comorbidity. Kecmanović M; Ristić AJ; Sokić D; Keckarević-Marković M; Vojvodić N; Ercegovac M; Janković S; Keckarević D; Savić-Pavićević D; Romac S Epilepsia; 2009 Jun; 50(6):1612-5. PubMed ID: 19170735 [TBL] [Abstract][Full Text] [Related]
30. [The relationship of dyssynergia cerebellaris myoclonica (Hunt) to myoclonus epilepsy (Unverricht-Lundborg)]. SEITZ D Dtsch Z Nervenheilkd; 1955; 173(2):111-22. PubMed ID: 14391125 [No Abstract] [Full Text] [Related]
39. [From gene to disease; progressive myoclonus epilepsy of Unverricht-Lundborg and mutations in the cystatin B gene]. de Haan GJ; Halley DJ; Deelen WH; Lindhout D Ned Tijdschr Geneeskd; 2002 May; 146(18):846-8. PubMed ID: 12038222 [TBL] [Abstract][Full Text] [Related]
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