Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain

JD Wood, JC MacMillan, PS Harper… - Human molecular …, 1996 - academic.oup.com
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the
expansion of a CAG repeat in a gene coding for a protein of unknown function. We have …
被引用次数：110 相关文章
[PDF] academia.edu

[PDF][PDF] Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain

JD Wood, JC MacMillan, PS Harper… - Human Molecular …, 1996 - academia.edu
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the
expansion of a CAG repeat in a gene coding for a protein of unknown function. We have …

[引用][C] Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain

JD Wood, JC MacMillan, PS Harper… - Human Molecular …, 1996 - elibrary.ru

Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain

JD Wood, JC MacMillan, PS Harper… - Human Molecular …, 1996 - orca.cardiff.ac.uk
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the
expansion of a CAG repeat in a gene coding for a protein of unknown function. We have …

Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain

JD Wood, JC MacMillan, PS Harper… - Human molecular …, 1996 - pubmed.ncbi.nlm.nih.gov
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the
expansion of a CAG repeat in a gene coding for a protein of unknown function. We have …

Partial Characterisation of Murine Huntingtin and Apparent Variations in the Subcellular Localisation of Huntingtin in Human, Mouse and Rat Brain.

JD Wood, JC MacMillan, PS Harper… - Human Molecular …, 1996 - search.ebscohost.com
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the
expansion of a CAG repeat in a gene coding for a protein of unknown function. We have …
[PDF] researchgate.net

[PDF][PDF] Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain

JD Wood, JC MacMillan, PS Harper… - Human Molecular …, 1996 - researchgate.net
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the
expansion of a CAG repeat in a gene coding for a protein of unknown function. We have …
[PDF] psu.edu

[PDF][PDF] Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain

JD Wood, JC MacMillan, PS Harper… - Human Molecular …, 1996 - Citeseer
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the
expansion of a CAG repeat in a gene coding for a protein of unknown function. We have …

[引用][C] Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain

JD WOOD, JC MACMILLAN… - Human molecular …, 1996 - pascal-francis.inist.fr
Partial characterisation of murine huntingtin and apparent variations in the subcellular
localisation of huntingtin in human, mouse and rat brain CNRS Inist Pascal-Francis CNRS …

Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain.

JD Wood, JC MacMillan, PS Harper… - Human Molecular …, 1996 - europepmc.org
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the
expansion of a CAG repeat in a gene coding for a protein of unknown function. We have …