Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
J Neural Transm (Vienna) ; 123(4): 451-3, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26695639

ABSTRACT

Several clinical phenotypes were associated with presenilin 1 (PSEN1) mutation in early-onset familial Alzheimer's disease (EOFAD). We report the clinical phenotype of two members of a familial dementia kindred who presented with EOFAD and early psychiatric syndrome as behavioral abnormalities. Sequence analysis of the index patient and his brother's PSEN1 transcript revealed a novel T > C transition in exon 4 which was determined as a missense substitution at position 248 of the coding sequence (cDNA. 248T > C).


Subject(s)
Alzheimer Disease/genetics , Mutation , Presenilin-1/genetics , Aged , Female , Humans , Male , Middle Aged , Mutation, Missense , Pedigree , Phenotype
SELECTION OF CITATIONS
SEARCH DETAIL
...