Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy”

Liknande verk

• Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy
  av: Lv, Yudan, et al.
  Publicerad: (2017)
• Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID
  av: Redler, Silke, et al.
  Publicerad: (2017)
• Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy
  av: Molinari, Florence, et al.
  Publicerad: (2005)
• Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13.
  av: Zara, F, et al.
  Publicerad: (2000)
• Cerebral Evoked Potentials in Familial Progressive Myoclonic Epilepsy
  av: Halliday, A. M.
  Publicerad: (1967)