Missense mutation in exon 11 (Codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer's disease and transmission study by mismatch enhanced allele specific amplification. Mutations in brief no. 141. Online. besancon@rockefeller1.univ.lyon1.fr.

Human mutation

Volumn 11, Issue 6, 1998, Pages 481-

  Besancon R ^a   Lorenzi, A ^a   Cruts, M ^a   Radawiec, S ^a   Sturtz, F ^a   Broussolle, E ^a   Chazot, G ^a   van Broeckhoven, C ^a   Chamba, G ^a   Vandenberghe, A ^a  

^a UNIVERSITÉ LYON 1   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; PRESENILIN 1; PSEN1 PROTEIN, HUMAN;

ALLELE; ALZHEIMER DISEASE; ARTICLE; BASE MISPAIRING; EXON; GENETIC SCREENING; GENETICS; HUMAN; MISSENSE MUTATION; ONSET AGE; PEDIGREE;

AGE OF ONSET; ALLELES; ALZHEIMER DISEASE; BASE PAIR MISMATCH; EXONS; GENETIC SCREENING; HUMANS; MEMBRANE PROTEINS; MUTATION, MISSENSE; PEDIGREE; PRESENILIN-1;

MLCS; MLOWN;

EID: 0032248908     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1098-1004(1998)11:6<481::aid-humu13>3.3.co;2-e     Document Type: Article

References (0)