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Juvenile Huntington's Disease: and other trinucleotide repeat disorders Oliver W J Quarrell
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Juvenile Huntington's Disease: and other trinucleotide repeat disorders
Oliver W J Quarrell
Huntington's disease (HD) is an inherited progressive neurodegenerative disorder. Although onset of HD usually occurs in adulthood, a small percentage of cases develop symptoms before 20 years of age (juvenile-onset Huntington's Disease or JHD). This book summarises, for the first time, the clinical and scientific knowledge available on JHD.
224 pages, 16 black and white line drawings and 10 photographs
| Medios de comunicación | Libros Hardcover Book (Libro con lomo y cubierta duros) |
| Publicado | 15 de marzo de 2009 |
| ISBN13 | 9780199236121 |
| Editores | Oxford University Press |
| Páginas | 222 |
| Dimensiones | 163 × 240 × 19 mm · 476 g |
| Lengua | Inglés |
| Editor | Barker, Roger A. (Reader in Clinical Neuroscience and Honorary Consultant Neurologist, University of Cambridge and Addenbrooke's Hospital, UK) |
| Editor | Brewer, Helen M. (Care Adviser - Juvenile Huntington's Disease, Huntington's Disease Association, England and Wales, UK) |
| Editor | Landwehrmeyer, G. Bernhard (Professor of Neurology at the University of Ulm, Germany and Chief Executive of the European Huntington's Disease Network) |
| Editor | Nance, Martha A. (Medical Director of the HDSA Center of Excellence, Hennepin County Medical Center, Minneapolis, USA and Adjunct Professor in the Department of Neurology at the University of Minnesota, USA) |
| Editor | Quarrell, Oliver W.J. (Consultant in Clinical Genetics at Sheffield Children's Hospital, and Vice-Chair of the Huntington's Disease Association, UK) |
| Editor | Squitieri, Ferdinando (, Director of the Neurogenetics Unit, IRCCS Neuromed and Centre for Rare diseases, Pozzilli, Italy) |
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