Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q

American Journal of Human Genetics

Volumn 58, Issue 6, 1996, Pages 1247-1253

  Virtaneva, K ^a   Miao, J ^a   Traskelin, A L ^a   Stone, N ^a   Warrington, J A ^a   Weissenbach, J ^a   Myers, R M ^a   Cox, D R ^a   Sistonen, P ^a   De la Chapelle, A ^a   Lehesjoki, A E ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHILD; CHROMOSOME 21Q; COSMID; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; GENETIC RECOMBINATION; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MYOCLONUS EPILEPSY; PRIORITY JOURNAL;

ADULT; BASE SEQUENCE; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 21; EPILEPSIES, MYOCLONIC; FEMALE; FINLAND; GENES, RECESSIVE; GENETIC MARKERS; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMORPHISM, GENETIC;

EID: 0029994692     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)