Juvenile Huntington's Disease: and other trinucleotide repeat disorders - Oliver W J Quarrell - Books - Oxford University Press - 9780199236121 - March 15, 2009
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Juvenile Huntington's Disease: and other trinucleotide repeat disorders

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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

Media Books     Hardcover Book   (Book with hard spine and cover)
Released March 15, 2009
ISBN13 9780199236121
Publishers Oxford University Press
Pages 222
Dimensions 163 × 240 × 19 mm   ·   476 g
Language English  
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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