Trinucleotide repeat length and progression of illness in Huntington's disease.

Author:

Kieburtz K,MacDonald M,Shih C,Feigin A,Steinberg K,Bordwell K,Zimmerman C,Srinidhi J,Sotack J,Gusella J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference11 articles.

1. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease;Andrew, S.E.; Goldberg, Y.P.; Kremer, B.;Nature,1993

2. Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15;Stine, O.C.; Pleasant, N.; Franz, M.L.; Abbott, M.H.; Foistein, S.E.; Ross, C.A.;Hum Molec Genet,1993

3. Mutation size and age at onset in _Huntington's disease;Craufurd, D.; Dodge, A.;J Med Genet,1993

4. Huntington's disease in Grampian region: correlation of the CAG repeat number and the age of onset of the disease;Simpson, S.A.; Davidson, M.J.; Barron, L.H.;J Med Genet; Molecular analysis and clinical correlations of the Huntington's disease mutation,1993

5. Duration of illness in Huntington's disease is not related to age at onset;Roos, R.A.C.; Hermans, J.; Vegter-van der Vlis, M.; van Ommen, G.J.B.; Bruyn, G.W.;J Neurol Neurosurg Psychiatry,1993

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