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Partners of mutation-carriers for Huntington's disease: forgotten persons?

✍ Scribed by Decruyenaere, Marleen; Evers-Kiebooms, Gerry; Boogaerts, Andrea; Demyttenaere, Koen; Dom, René; Fryns, Jean-Pierre

Book ID
110026366
Publisher
Nature Publishing Group
Year
2005
Tongue
English
Weight
109 KB
Volume
13
Category
Article
ISSN
1018-4813

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## Abstract Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by a CAG repeat expansion in the __IT‐15__ gene; however, it remains unknown how the mutation leads to selective neurodegeneration. Several lines of evidence suggest impaired mitochondrial f