P-8. Molecular genetic studies of Charcot-Marie-Tooth disease in the Cypriot population

समान संसाधन

• P-7. Huntington’s disease in the Cypriot population: direct molecular diagnosis since 1994
  द्वारा: Georghiou, A, और अन्य
  प्रकाशित: (2009)
• P-3. Investigation of the spinocerebellar ataxia type 10 mutation in the Cypriot population
  द्वारा: Votsi, C, और अन्य
  प्रकाशित: (2009)
• P-4. Investigation of Cypriot families with autosomal recessive spinocerebellar ataxia (arsca) by linkage analysis at known arsca genes/loci
  द्वारा: Votsi, C, और अन्य
  प्रकाशित: (2009)
• P-2. Friedreich’s ataxia carrier screening in the population originating from the Paphos district of Cyprus
  द्वारा: Koutsou, P, और अन्य
  प्रकाशित: (2009)
• A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease
  द्वारा: Nicolaou, Paschalis, और अन्य
  प्रकाशित: (2013)