The expanded CAG repeat associated with juvenile Huntington disease shows a common origin of most or all neurons and glia in human cerebrum

Author:

Kahlem Pascal,Djian Philippe

Publisher

Elsevier BV

Subject

General Neuroscience

Reference21 articles.

1. CAG expansion affects the expression of mutant huntingtin in the Huntington's disease brain;Aronin;Neuron,1995

2. Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1;Chong;Nat. Genet.,1995

3. A self-renewing multipotential stem cell in embryonic rat cerebral cortex;Davis;Nature,1994

4. De Koning Gans;De Rooij;P.A.M., Roos, R.A.C., Van Ommen, G.-J.B. and Den Dunnen, J.T., Somatic expansion of the (CAG)n repeat in Huntington disease brains, Hum. Genet.,1995

5. Ultrastructural immunocytochemistry of glia cells;Goto;Double labeling studies using LR White embedding and colloidal gold, Histochemistry,1987

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