Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1995.tb03941.x/fullpdf
Reference19 articles.
1. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease;Andrew;Nature Genetics,1993
2. Intergenerational stability of the myotonic dystrophy protomutation;Barceló;Hum Mol Genet,1993
3. Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range;Rooij;J Med Genet,1993
4. Trinucleotide repeat length instability and age of onset in Huntington's disease;Duyao;Nature Genetics,1993
5. Variation of the CGG repeat at the Fragile X site results in genetic instability: resolution of the Sherman paradox;Fu;Cell,1991
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2. Association between sex and Huntington’s disease: an updated review on symptomatology and prognosis of neurodegenerative disorders;Wiener Medizinische Wochenschrift;2022-06-20
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4. CAG repeat instability in embryonic stem cells and derivative spermatogenic cells of transgenic Huntington’s disease monkey;Journal of Assisted Reproduction and Genetics;2021-02-20
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