Lack of implication for calhm1 p86l common variation in italian patients with early and late onset alzheimer's disease

Journal of Alzheimer's Disease

Volumn 20, Issue 1, 2010, Pages 37-41

  Nacmias, Benedetta ^a   Tedde, Andrea ^a   Bagnoli, Silvia ^a   Lucenteforte, Ersilia ^a   Cellini, Elena ^a   Piaceri, Irene ^a   Guarnieri, Bianca Maria ^b   Bessi, Valentina ^a   Bracco, Laura ^a   Sorbi, Sandro ^a  

^a UNIVERSITY OF FLORENCE   (Italy)

^b Casa di Cura Villa Serena   (Italy)

Author keywords

Alzheimer's disease; apolipoprotein E; calcium homeostasis modulator 1; genetic variation

Indexed keywords

LEUCINE; PROLINE;

AGED; ALLELE; ALZHEIMER DISEASE; ARTICLE; CALCIUM HOMEOSTASIS MODULATOR 1 GENE; CONTROLLED STUDY; DNA POLYMORPHISM; FAMILY HISTORY; FEMALE; GENE; GENE FREQUENCY; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 77954497203     PISSN: 13872877     EISSN: None     Source Type: Journal    
DOI: 10.3233/JAD-2010-1345     Document Type: Article

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