The human FE65 gene: Genomic structure and an intronic biallelic polymorphism associated with sporadic dementia of the Alzheimer type

Human Genetics

Volumn 103, Issue 3, 1998, Pages 295-303

  Hu, Qubai ^a   Kukull, Walter A ^a   Bressler, Steven L ^a   Gray, Matthew D ^a   Cam, Judith A ^a   Larson, Eric B ^a   Martin, George M ^a   Deeb, Samir S ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID BETA PROTEIN; AMYLOID PRECURSOR PROTEIN; COMPLEMENTARY DNA;

AGED; ALZHEIMER DISEASE; AMINO ACID SUBSTITUTION; ARTICLE; BINDING SITE; CAUCASIAN; CONSENSUS SEQUENCE; CONTROLLED STUDY; DNA POLYMORPHISM; DNA SEQUENCE; DONOR SITE; EXON; FEMALE; GENE AMPLIFICATION; GENE EXPRESSION; GENE MAPPING; GENE SEQUENCE; GENETIC SCREENING; GENOTYPE; HUMAN; INTERNALIZATION; INTRON; MAJOR CLINICAL STUDY; MALE; MULTIVARIATE ANALYSIS; NORMAL HUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN METABOLISM; PROTEIN PROTEIN INTERACTION; SINGLE STRAND CONFORMATION POLYMORPHISM;

AGED; ALLELES; ALZHEIMER DISEASE; BASE SEQUENCE; CLONING, MOLECULAR; DEMENTIA; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXONS; FEMALE; HUMANS; INTRONS; MALE; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; NUCLEAR PROTEINS; POLYMORPHISM, GENETIC; SEQUENCE ANALYSIS, DNA;

EID: 0031710443     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050820     Document Type: Article

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