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Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

Aziz, NA; Jurgens, CK; Landwehrmeyer, GB; van Roon-Mom, WMC; van Ommen, GJB; Stijnen, T; Roos, RAC; ... Tidswell, K; + view all (2009) Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease. NEUROLOGY , 73 (16) pp. 1280-1285. 10.1212/WNL.0b013e3181bd1121.

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Type: Article
Title: Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease
DOI: 10.1212/WNL.0b013e3181bd1121
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, WILD-TYPE HUNTINGTIN, CAG REPEAT LENGTH, AGE-OF-ONSET, CELLULAR TOXICITY, WEIGHT-LOSS, TRANSCRIPTION, GENE, MODEL, HD
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Clinical and Movement Neurosciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases
URI: http://discovery.ucl.ac.uk/id/eprint/1487567
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