DCTN1 F52L mutation case of Perry syndrome with progressive supranuclear palsy-like tauopathy
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference24 articles.
1. Hereditary mental depression and Parkinsonism with taurine deficiency;Perry;Arch. Neurol.,1975
2. Rapidly progressive familial parkinsonism with central hypoventilation, depression and weight loss (Perry syndrome)–a literature review;Wider;Park. Relat. Disord.,2008
3. Familial parkinsonism with depression: a clinicopathological study;Bhatia;Ann. Neurol.,1993
4. Japanese family with parkinsonism, depression, weight loss, and central hypoventilation;Tsuboi;Neurology,2002
5. DCTN1 mutations in Perry syndrome;Farrer;Nat. Genet.,2009
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