A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

Nature Genetics

Volumn 13, Issue 4, 1996, Pages 464-468

  Sawcer, S ^a   Jones, H B ^a   Feakes, R ^a   Gray, J ^a   Smaldon, N ^a   Chataway, J ^a   Robertson, N ^a   Clayton, D ^a   Goodfellow, P N ^a   Compston, A ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 17Q; CHROMOSOME 6P; GENETIC LINKAGE; GENETIC MODEL; HEREDITY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MAJOR HISTOCOMPATIBILITY COMPLEX; MULTIPLE SCLEROSIS; PREVALENCE; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 6; FEMALE; GENE FREQUENCY; GENETIC MARKERS; HUMANS; LIKELIHOOD FUNCTIONS; LINKAGE DISEQUILIBRIUM; MALE; MICROSATELLITE REPEATS; MULTIPLE SCLEROSIS;

EID: 15844368830     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0896-464     Document Type: Article

References (0)