Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3 [5] (multiple letters)

American Journal of Human Genetics

Volumn 67, Issue 1, 2000, Pages 262-263

  Lesperance, Marci M ^a   Burmeister, Margit ^a,b   Kambouris, Marios ^c,d   Meyer, Brian F ^c  

^a UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

^c KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^d YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; CHROMOSOME 4P; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENETIC ANALYSIS; GENETIC RECOMBINATION; GENOME; GENOTYPE; HAPLOTYPE; HOMOZYGOSITY; HUNTINGTON CHOREA; LETTER; PRIORITY JOURNAL;

EID: 0033910386     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302975     Document Type: Letter

References (2)

1. M Kambouris S Bohlega A Al-Tahan BF Meyer Localization of the gene for a novel autosomal recessive neurodegenerative Huntington-like disorder to 4p15.3 Am J Hum Genet 66 2000 445 452
2. ES Lander NJ Schork Genetic dissection of complex traits Science 265 1994 2037 2048