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Oculomotor defects in patients with Huntington's disease and their offspring

✍ Scribed by H. Collewijn; L.N. Went; E.P. Tamminga; M. Vegter-Van der Vlis

Book ID
118930563
Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
880 KB
Volume
86
Category
Article
ISSN
0022-510X

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πŸ“œ SIMILAR VOLUMES

Complex I Defect in muscle from patients
Complex I Defect in muscle from patients with Huntington's disease
✍ Dr JoaquΓ­n Arenas; Yolanda Campos; RenΓ© Ribacoba; Miguel A. MartΓ­n; Juan C. Rubi πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 439 KB πŸ‘ 2 views

We found a variable defect of complex I of the mitochondrial respiratory chain, ranging in severity from 25% to 63% of control values, in muscle of patients with Huntington's disease (HD). The most severe defect was observed in the patient with the greatest expansion of CAG triplets. Muscle morpholo