Counting CAG repeats in the Huntington’s disease gene by restriction endonuclease EcoP15I cleavage

Huntington’s disease (HD) is a progressive neurodegenerative disorder with autosomal-dominant inheritance. The disease is caused by a CAG trinucleotide repeat expansion located in the first exon of the HD gene. The CAG repeat is highly polymorphic and varies from 6 to 37 repeats on chromosomes of un...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Möncke-Buchner, Elisabeth, Reich, Stefanie, Mücke, Merlind, Reuter, Monika, Messer, Walter, Wanker, Erich E., Krüger, Detlev H.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2002
Konular:
NAR Methods Online
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC134256/
https://ncbi.nlm.nih.gov/pubmed/12177311
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller