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Quoted phrase not found in phrase index: "Huntington disease-like 3"
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A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.
Xiang F, Almqvist EW, Huq M, Lundin A, Hayden MR, Edström L, Anvret M, Zhang Z. Xiang F, et al. Am J Hum Genet. 1998 Nov;63(5):1431-8. doi: 10.1086/302093. Am J Hum Genet. 1998. PMID: 9792871 Free PMC article.
Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterized by motor disturbance, cognitive loss, and psychiatric manifestations. The disease is associated with a CAG trinucleotide-repeat expansion in the Huntington gene (IT15) on chrom
Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterized by motor disturbance, cognitive loss, and p
Feeding dystonia in McLeod syndrome.
Gantenbein AR, Damon-Perrière N, Bohlender JE, Chauveau M, Latxague C, Miranda M, Jung HH, Tison F. Gantenbein AR, et al. Mov Disord. 2011 Sep;26(11):2123-6. doi: 10.1002/mds.23843. Epub 2011 Jun 28. Mov Disord. 2011. PMID: 21714011
BACKGROUND: The X-linked McLeod syndrome belongs to the group of neuroacanthocytosis syndromes and has a Huntington-disease-like phenotype with a choreatic movement disorder, cognitive alterations, and psychiatric symptoms. ...RESULTS: The 3 patients with McL …
BACKGROUND: The X-linked McLeod syndrome belongs to the group of neuroacanthocytosis syndromes and has a Huntington-disease- …
A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion.
Margolis RL, O'Hearn E, Rosenblatt A, Willour V, Holmes SE, Franz ML, Callahan C, Hwang HS, Troncoso JC, Ross CA. Margolis RL, et al. Ann Neurol. 2001 Sep;50(3):373-80. Ann Neurol. 2001. PMID: 11558794 Corrected and republished.
Huntington's disease (HD) is an autosomal dominant disorder characterized by abnormalities of movement, cognition, and emotion and selective atrophy of the striatum and cerebral cortex. ...Cloning the causative CAG expansion mutation for this new disease, which we h
Huntington's disease (HD) is an autosomal dominant disorder characterized by abnormalities of movement, cognition, and emotion