Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: Linkage disequilibrium allows high resolution mapping

Human Molecular Genetics

Volumn 2, Issue 8, 1993, Pages 1229-1234

  Lehesjokl, Anna Ellna ^a,b   Koskiniemi, Marjaleena ^a,c   Norio, Reljo ^a,d   Tirrito, Salvatore ^a,b   Sistonen, Perttl ^a,e   Lander, Eric ^a,f   Chapelle, Albert De La ^a,b  

^a FOLKHÄLSAN INSTITUTE OF GENETICS   (Finland)

^b UNIVERSITY OF HELSINKI   (Finland)

^c Finnish Population and Family Welfare Federation ^*  (Finland)

^d FINNISH RED CROSS BLOOD SERVICE   (Finland)

^e Whrtehead Institute for Biomedical Research ^*  (United Kingdom)

^f MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 21; CHROMOSOME MAP; CLINICAL ARTICLE; CONTROLLED STUDY; CROSSOVER PROCEDURE; FAMILY STUDY; FINLAND; GENE LINKAGE DISEQUILIBRIUM; GENE LOCATION; GENETIC DISTANCE; HUMAN; MARKER GENE; MYOCLONUS EPILEPSY; POPULATION GENETICS;

ALLELES; BASE SEQUENCE; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 21; DNA PRIMERS; DNA, SATELLITE; EPILEPSIES, MYOCLONIC; FEMALE; HAPLOTYPES; HUMAN; LINKAGE DISEQUILIBRIUM; MALE; MOLECULAR SEQUENCE DATA; NUCLEAR FAMILY; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RECOMBINATION, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0027236091     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/2.8.1229     Document Type: Article

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