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P1‐123: VERY YOUNG ONSET AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE WITH SPASTIC PARAPARESIS DUE TO A NOVEL (F388S) PSEN1 MUTATION
Author(s) -
Ringman John M.,
Dorrani Naghmeh,
Signer Rebecca,
Martinez-Agosto Julian,
Lee Hane,
Douine Emilie,
Qiao Yuchuan,
Wang Junyan,
Shi Yonggang,
D'Orazio Lina,
Cederbaum Stephan,
Nelson Stanley,
Chui Helena C.
Publication year - 2019
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2019.06.678
Subject(s) - psen1 , hereditary spastic paraplegia , proband , exome sequencing , spasticity , medicine , dementia , pediatrics , mutation , age of onset , disease , pathology , alzheimer's disease , genetics , presenilin , biology , physical medicine and rehabilitation , gene , phenotype