期刊
NEUROLOGY
卷 64, 期 2, 页码 377-379出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/01.WNL.0000149761.70566.3E
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资金
- NIA NIH HHS [K08 AG 22228] Funding Source: Medline
The occurrence of an APP T174I mutation is described in a large American family of African descent with Alzheimer disease. The clinical characteristics were an unusually early onset of disease (early 30s), similar to a previously reported age at onset of this mutation in an Austrian family. Distinct from that family, seizures and myoclonus were prominent features of the disease in this kindred.
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