An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder

Epilepsia

Volumn 49, Issue 6, 2008, Pages 1086-1090

  Kugler, Steven L ^a   Bali, Bhavna ^b   Lieberman, Philip ^c   Strug, Lisa ^b   Gagnon, Bernadine ^d   Murphy, Peregrine L ^b   Clarke, Tara ^b   Greenberg, David A ^b,d   Pal, Deb K ^b,d  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b Columbia University ^*  (United States)

^c BROWN UNIVERSITY   (United States)

^d Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

Broca; Dyspraxia; Linkage; Oromotor; Pedigree; Speech

Indexed keywords

ADOLESCENT; ADULT; APRAXIA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 11P; CHROMOSOME 15Q; CHROMOSOME 16P; CHROMOSOME ANALYSIS; CHROMOSOME XQ; CLINICAL ARTICLE; CLINICAL FEATURE; COGNITIVE DEFECT; FEMALE; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MALE; PEDIGREE; PRIORITY JOURNAL; ROLANDIC EPILEPSY; SCHOOL CHILD; SPEECH DISORDER; SPIKE WAVE;

ADULT; APRAXIAS; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME MAPPING; EPILEPSY, ROLANDIC; EVOKED POTENTIALS; GENES, DOMINANT; GENETIC HETEROGENEITY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MENTAL RETARDATION; MICROSATELLITE REPEATS; NEUROLOGIC EXAMINATION; PEDIGREE; PHENOTYPE; SOUND SPECTROGRAPHY; SPEECH PRODUCTION MEASUREMENT; TEMPORAL LOBE;

EID: 44849094237     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2007.01517.x     Document Type: Article

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