Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease-Reference-Cited by-同舟云学术

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

Published:1993-08 Issue:4 Volume:4 Page:393-397
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Snell Russell G.,MacMillan John C.,Cheadle Jeremy P.,Fenton Iain,Lazarou Lazarus P.,Davies Peter,MacDonald Marcy E.,Gusella James F.,Harper Peter S.,Shaw Duncan J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0893-393.pdf

Reference23 articles.

1. Harper, P.S. Huntington's disease. (W.B. Saunders, London, 1991).

2. The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72, 971–983 (1993).

3. Brook, J.D. et al. Molecular basis of Myotonic Dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 68, 799–808 (1992).

4. Verkerk, A.J.M.H. et al. Identification of a gene (FMR-1) containing a CCG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65, 905–914 (1991).

5. LaSpada, A.R. et al. Androgen receptor gene mutations in X-linked spinal and bulbar muscular dystrophy. Nature 352, 77–79 (1991).

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