Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation [16]

Lancet

Volumn 347, Issue 9014, 1996, Pages 1560-

  Rossor, M N ^a   Fox, N C ^a   Beck, J ^a   Campbell, T C ^a   Collinge, J ^a  

^a NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ALZHEIMER DISEASE; CASE REPORT; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; GENE MUTATION; HUMAN; LETTER; PEDIGREE; PRIORITY JOURNAL;

EID: 0029899593     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(96)90715-1     Document Type: Letter

References (4)

1. R. Sherrington El Rogaev Y. Lian Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease Nature 375 1995 754 760
2. Rf Clarke M. Hutton Ra Fuldner The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families Nat Genet 11 1995 219 222
3. M. Cruts H. Backhovens Sy Wang Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14224.3 Hum Molec Genet 4 1995 2363 2371
4. S. Sorbi B. Nacimias P. Forleo Epistatic effect of APP 717: mutation and apolipoprotein E genotype in familial Alzheimer's disease Ann Neurol 38 1995 124 127