Comment on

• A novel locus for inherited myoclonus-dystonia on 18p11.

  Grimes DA, Han F, Lang AE, St George-Hyssop P, Racacho L, Bulman DE. Grimes DA, et al. Neurology. 2002 Oct 22;59(8):1183-6. doi: 10.1212/wnl.59.8.1183. Neurology. 2002. PMID: 12391345
• 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. Doheny DO, et al. Neurology. 2002 Oct 22;59(8):1187-96. doi: 10.1212/wnl.59.8.1187. Neurology. 2002. PMID: 12391346
• Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome.

  Leuzzi V, Carducci C, Carducci C, Cardona F, Artiola C, Antonozzi I. Leuzzi V, et al. Neurology. 2002 Oct 22;59(8):1241-3. doi: 10.1212/wnl.59.8.1241. Neurology. 2002. PMID: 12391354
• Clinical findings of a myoclonus-dystonia family with two distinct mutations.

  Doheny D, Danisi F, Smith C, Morrison C, Velickovic M, De Leon D, Bressman SB, Leung J, Ozelius L, Klein C, Breakefield XO, Brin MF, Silverman JM. Doheny D, et al. Neurology. 2002 Oct 22;59(8):1244-6. doi: 10.1212/wnl.59.8.1244. Neurology. 2002. PMID: 12391355