Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene
- PMID: 8755937
- PMCID: PMC1914734
Item in Clipboard
Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene
Am J Hum Genet.
1996 Aug.
No abstract available
Similar articles
-
Two novel single-base-pair substitutions adjacent to the CAG repeat in the huntington disease gene (IT15): implications for diagnostic testing.Am J Hum Genet. 1999 Jan;64(1):323-6. doi: 10.1086/302209. Am J Hum Genet. 1999. PMID: 9915978 Free PMC article. No abstract available.
-
Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standards.Mol Cell Probes. 1999 Aug;13(4):283-9. doi: 10.1006/mcpr.1999.0248. Mol Cell Probes. 1999. PMID: 10441201
-
[Molecular analysis of the IT15 gene in 79 Spanish families with Huntington's disease: diagnostic confirmation and presymptomatic diagnosis].Med Clin (Barc). 1997 May 10;108(18):687-90. Med Clin (Barc). 1997. PMID: 9324583 Spanish.
-
Huntington disease: clinical, genetic, and social aspects.J Geriatr Psychiatry Neurol. 1998 Summer;11(2):61-70. doi: 10.1177/089198879801100204. J Geriatr Psychiatry Neurol. 1998. PMID: 9877527 Review.
-
[Huntington's disease].Ryoikibetsu Shokogun Shirizu. 2003;(40):261-4. Ryoikibetsu Shokogun Shirizu. 2003. PMID: 14626115 Review. Japanese. No abstract available.
Cited by
-
Oxytosis/Ferroptosis in Neurodegeneration: the Underlying Role of Master Regulator Glutathione Peroxidase 4 (GPX4).Mol Neurobiol. 2024 Mar;61(3):1507-1526. doi: 10.1007/s12035-023-03646-8. Epub 2023 Sep 19. Mol Neurobiol. 2024. PMID: 37725216 Review.
-
A probable cis-acting genetic modifier of Huntington disease frequent in individuals with African ancestry.HGG Adv. 2022 Jul 11;3(4):100130. doi: 10.1016/j.xhgg.2022.100130. eCollection 2022 Oct 13. HGG Adv. 2022. PMID: 35935919 Free PMC article.
-
Genetic modifiers of Huntington disease differentially influence motor and cognitive domains.Am J Hum Genet. 2022 May 5;109(5):885-899. doi: 10.1016/j.ajhg.2022.03.004. Epub 2022 Mar 23. Am J Hum Genet. 2022. PMID: 35325614 Free PMC article.
-
Huntington's disease: nearly four decades of human molecular genetics.Hum Mol Genet. 2021 Oct 1;30(R2):R254-R263. doi: 10.1093/hmg/ddab170. Hum Mol Genet. 2021. PMID: 34169318 Free PMC article. Review.
-
Huntington's Disease Pathogenesis: Two Sequential Components.J Huntingtons Dis. 2021;10(1):35-51. doi: 10.3233/JHD-200427. J Huntingtons Dis. 2021. PMID: 33579862 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical