Myoclonic encephalopathy in the CDKL5 gene mutation

Clinical Neurophysiology

Volumn 117, Issue 1, 2006, Pages 223-227

  Buoni, Sabrina ^a   Zannolli, Raffaella ^a   Colamaria, Vito ^b   Macucci, Francesca ^a   Di Bartolo, Rosanna M ^a   Corbini, Letizia ^a   Orsi, Alessandra ^c   Zappella, Michele ^c   Hayek, Joseph ^c  

^a UNIVERSITY OF SIENA   (Italy)

^b Pediatrics Neuropsychiatric Service   (Italy)

^c UNIVERSITY HOSPITAL OF SIENA   (Italy)

Author keywords

CDKL5 gene; Myoclonic encephalopathy

Indexed keywords

ANAMNESIS; BRAIN DISEASE; CASE REPORT; CDKL5 GENE; ELECTROENCEPHALOGRAM; EPILEPSY; FEMALE; GENE; GENE DELETION; GENE MUTATION; HUMAN; INFANTILE SPASM; MYOCLONUS; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; RETT SYNDROME; REVIEW; SCHOOL CHILD; SEIZURE;

EID: 30744452971     PISSN: 13882457     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinph.2005.09.008     Document Type: Article

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