Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

EJ Slow, J van Raamsdonk, D Rogers… - Human molecular …, 2003 - academic.oup.com
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder
characterized by motor, psychiatric and cognitive deficits and striatal atrophy associated with …
被引用次数：951 相关文章
[PDF] researchgate.net

[PDF][PDF] Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

EJ Slow, J van Raamsdonk, D Rogers… - Human Molecular …, 2003 - researchgate.net
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder
characterized by motor, psychiatric and cognitive deficits and striatal atrophy associated with …
[PDF] archive.org

[PDF][PDF] Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

EJ Slow, J van Raamsdonk, D Rogers… - Human Molecular …, 2003 - scholar.archive.org
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder
characterized by motor, psychiatric and cognitive deficits and striatal atrophy associated with …

Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

EJ Slow, J van Raamsdonk… - Human molecular …, 2003 - pubmed.ncbi.nlm.nih.gov
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder
characterized by motor, psychiatric and cognitive deficits and striatal atrophy associated with …

[引用][C] Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

EJ SLOW, J VAN RAAMSDONK, XJ LI… - Human molecular …, 2003 - pascal-francis.inist.fr
Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease CNRS Inist
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Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease.

EJ Slow, J van Raamsdonk, D Rogers… - Human Molecular …, 2003 - europepmc.org
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder
characterized by motor, psychiatric and cognitive deficits and striatal atrophy associated with …
[PDF] psu.edu

[PDF][PDF] Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

EJ Slow, J van Raamsdonk, D Rogers… - Human Molecular …, 2003 - Citeseer
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder
characterized by motor, psychiatric and cognitive deficits and striatal atrophy associated with …

Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease.

EJ Slow, J van Raamsdonk, D Rogers… - Human Molecular …, 2003 - search.ebscohost.com
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder
characterized by motor, psychiatric and cognitive deficits and striatal atrophy associated with …
[PDF] academia.edu

[PDF][PDF] Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

EJ Slow, J van Raamsdonk, D Rogers… - Human Molecular …, 2003 - academia.edu
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder
characterized by motor, psychiatric and cognitive deficits and striatal atrophy associated with …

Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

EJ Slow, J van Raamsdonk, D Rogers… - Human Molecular …, 2003 - elibrary.ru
An expanded CAG repeat is the underlying genetic defect in Huntington disease, a disorder
characterized by motor, psychiatric and cognitive deficits and striatal atrophy associated with …