Common SNP-Based Haplotype Analysis of the 4p16.3 Huntington Disease Gene Region - Lee, Jong-Min; Gillis, Tammy; Mysore, Jayalakshmi Srinidhi; Ramos, Eliana Marisa; Myers, Richard H.; Hayden, Michael R.; Morrison, Patrick J.; Nance, Martha; Ross, Christopher A.; Margolis, Russell L.; Squitieri, Ferdinando; Griguoli, Annamaria; et al. (American journal of human genetics, 2012)
Keywords: Age of Onset; Alleles; Biological and medical sciences; Case-Control Studies; Chromosomes, Human, Pair 4; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; Founder Effect; Fundamental and applied biological sciences. Psychology; General aspects. Genetic counseling; Genetic disorders; Genetics of eukaryotes. Biological and molecular evolution; Genome-Wide Association Study - methods; Haplotypes; Humans; Huntington Disease - genetics; Medical genetics; Medical sciences; Molecular and cellular biology; Motor ability; Mutation; Neurology; Pathogenesis; Polymorphism; Polymorphism, Single Nucleotide; Trinucleotide Repeats; Human; Nervous system diseases; Gene; Central nervous system disease; Huntington disease; Genetics; Degenerative disease; Single nucleotide polymorphism; Haplotype; Genetic disease; Cerebral disorder; Extrapyramidal syndrome