Article ID Journal Published Year Pages File Type
10745144 Parkinsonism & Related Disorders 2014 6 Pages PDF
Abstract
Families with such complex phenotypes rarely occur. They are usually associated with MAPT mutations; however, in this family, MAPT mutations have been excluded, implicating another causative gene or genes. Further genetic studies on this family may eventually disclose the etiology.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
Authors
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