Another rett patient with a Typical Angelman EEG [3] (multiple letters)

Epilepsia

Volumn 44, Issue 6, 2003, Pages 873-874

  Valente, Kette D ^a   Laan, Laura A E M ^b   Vein, Alla A ^b  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AMPLITUDE MODULATION; CASE REPORT; DEVELOPMENTAL DISORDER; DISEASE SEVERITY; ELECTROENCEPHALOGRAM; FEMALE; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; GENOTYPE; HUMAN; LETTER; PHENOTYPE; PRIORITY JOURNAL; RETT SYNDROME; SCHOOL CHILD;

AGE FACTORS; ANGELMAN SYNDROME; CHROMOSOMAL PROTEINS, NON-HISTONE; DIAGNOSIS, DIFFERENTIAL; DNA-BINDING PROTEINS; ELECTROENCEPHALOGRAPHY; GENOTYPE; HUMANS; INFANT; METHYL-CPG-BINDING PROTEIN 2; MUTATION; PHENOTYPE; REPRESSOR PROTEINS; RETT SYNDROME;

EID: 0038579245     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1528-1157.2003.04803_3.x     Document Type: Letter

References (0)