Magnetic resonance imaging of Huntington's disease: preparing for clinical trials

The known genetic mutation causing Huntington's disease (HD) makes this disease an important model to study links between gene and brain function. An autosomal dominant family history and the availability of a sensitive and specific genetic test allow pre-clinical diagnosis many years before th...

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Detalles Bibliográficos
Autores principales: Klöppel, S., Henley, S.M., Hobbs, N.Z., Wolf, R.C., Kassubek, J., Tabrizi, S.J., Frackowiak, R.S.J.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science 2009
Materias:
Neurological Disorder
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771270/
https://www.ncbi.nlm.nih.gov/pubmed/19409230
http://dx.doi.org/10.1016/j.neuroscience.2009.01.045

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771270/
https://www.ncbi.nlm.nih.gov/pubmed/19409230
http://dx.doi.org/10.1016/j.neuroscience.2009.01.045

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