X-linked myoclonic epilepsy with spasticity and intellectual disability: Mutation in the homeobox gene ARX

Neurology

Volumn 59, Issue 3, 2002, Pages 348-356

  Scheffer, I E ^a,b,c,h   Wallace, R H ^d   Phillips, F L ^a   Hewson, P ^e   Reardon, K ^f   Parasivam, G ^a   Stromme, P ^d   Berkovic, S F ^a,b   Gecz, J ^d,g   Mulley, J C ^d  

^a UNIVERSITY OF MELBOURNE   (Australia)

^b ROYAL CHILDREN'S HOSPITAL   (Australia)

^c MONASH MEDICAL CENTRE   (Australia)

^d WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^e BARWON HEALTH   (Australia)

^f ST VINCENT S HOSPITAL   (Australia)

^g UNIVERSITY OF ADELAIDE   (Australia)

^h AUSTIN HEALTH   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; ARX GENE; ATAXIA; CHILD; CLINICAL ARTICLE; ELECTROENCEPHALOGRAM; FAMILIAL DISEASE; GENE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENOTYPE PHENOTYPE CORRELATION; HOMEOBOX; HUMAN; HYPERREFLEXIA; HYPSARRHYTHMIA; INTELLECTUAL IMPAIRMENT; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; MYOCLONUS EPILEPSY; PRIORITY JOURNAL; SPASTICITY; SYNDROME; X CHROMOSOME LINKED DISORDER; X LINKED MYOCLONIC EPILEPSY WITH SPASTICITY AND INTELLECTUAL DISABILITY;

EID: 0037072260     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.59.3.348     Document Type: Article

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