Gametic but not somatic instability of CAG repeat length in Huntington's disease.

Author:

MacDonald M E,Barnes G,Srinidhi J,Duyao M P,Ambrose C M,Myers R H,Gray J,Conneally P M,Young A,Penney J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference5 articles.

1. Trinucleotide repeat length: instability and age of onset in Huntington's disease;Duyao, M.P.; Ambrose, C.M.; Myers, R.H.;Nature-Geniet,1993

2. Relationship between variation trinucleotide repeat in Huntington's expansion disease. aNnadtiuprheenotGeynp, iect;Snell, R.G.; MacMillan, J.C.; Cheadle, J.P.; ct al,1993

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

4. Fragile-X syndrome: Huunmi)qzueGetgieentet1i9c9s2; o5f0:th9e68h-e8r0i.table unstable clement. Am) _7 in fragile X syndrome and HD suggests that 12;Yu, S.; Mulley, J.; Loesch, D.;Cell; Molecular trinucleotide repeat expansion in these two disorders might result from fundamentally different mechanisms. A detailed analysis of repeat instability in each of the other disorders b(aCsTisGo)f mvotonic repeat at dtyhsetr3'opehny:d eoxfpaanstiraonnscorfiapttreinncucoldeiontgidea protein kinase family member,1992

5. Detection of an unstable myotonic fdryasgtmreonpthy.ofNDatNuiAre specific to individuals;Buxton, J.; Shelburne, P.; Davies, J.,1992

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