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P3‐224: Clinical phenotype of familial Alzheimer's disease caused by the H163R presenilin 1 mutation
Author(s) -
Gómez-Tortosa Estrella,
Manzano Sagrario,
Muñoz David G.,
Sainz M. José,
Jiménez-Huete Adolfo,
Barquero M. Sagrario,
Baron Manuel,
Jimenez-Escrig Adriano
Publication year - 2008
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.2008.05.1791
Subject(s) - apathy , presenilin , proband , psen1 , dementia , disease , psychology , context (archaeology) , medicine , neuroscience , alzheimer's disease , genetics , mutation , pathology , biology , gene , paleontology