Non-ceruloplasmin bound copper and: ATP7B gene variants in Alzheimer's disease

Metallomics

Volumn 8, Issue 9, 2016, Pages 863-873

  Squitti, R ^a   Siotto, M ^b   Arciello, M ^c   Rossi, L ^c,d  

^a IRCCS ISTITUTO CENTRO SAN GIOVANNI DI DIO FATEBENEFRATELLI   (Italy)

^b IRCCS FONDAZIONE DON CARLO GNOCCHI   (Italy)

^c UNIVERSITY OF ROME TOR VERGATA   (Italy)

^d NATIONAL INSTITUTE OF BIOSTRUCTURES AND BIOSYSTEMS   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BIOSYNTHESIS; BODY FLUIDS; COPPER; GENES; POLYMORPHISM; PROTEINS;

ALZHEIMER'S DISEASE; COPPER PROTEINS; GENETIC DEFECTS; MOLECULAR MECHANISM; NEURODEGENERATION; NEUROLOGICAL DISORDERS; SINGLE NUCLEOTIDE POLYMORPHISMS; WILSON'S DISEASE;

NEURODEGENERATIVE DISEASES;

CERULOPLASMIN; COPPER; WILSON DISEASE PROTEIN; ATP7B PROTEIN, HUMAN; COPPER EXPORTING ADENOSINE TRIPHOSPHATASE;

ALZHEIMER DISEASE; COPPER METABOLISM; GENE MUTATION; GENETIC VARIABILITY; HOMEOSTASIS; HUMAN; MAMMAL; NONHUMAN; PRIORITY JOURNAL; REVIEW; RISK FACTOR; SERUM; SINGLE NUCLEOTIDE POLYMORPHISM; WILSON DISEASE; GENETICS; METABOLISM; PATHOLOGY;

ALZHEIMER DISEASE; CERULOPLASMIN; COPPER; COPPER-TRANSPORTING ATPASES; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84988328409     PISSN: 17565901     EISSN: 1756591X     Source Type: Journal    
DOI: 10.1039/c6mt00101g     Document Type: Review

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