Genetic contribution to iron status: SNPs related to iron deficiency anaemia and fine mapping of CACNA2D3 calcium channel subunit

Blood Cells, Molecules, and Diseases

Volumn 55, Issue 4, 2015, Pages 273-280

  Baeza Richer, Carlos ^a   Arroyo Pardo, Eduardo ^a   Blanco Rojo, Ruth ^b   Toxqui, Laura ^c   Remacha, Angel ^d   Vaquero, M Pilar ^c   López Parra, Ana M ^a  

^a SCHOOL OF MEDICINE   (Spain)

^b HOSPITAL UNIVERSITARIO REINA SOFÍA   (Spain)

^c INSTITUTE OF FOOD SCIENCE   (Spain)

^d HOSPITAL DE LA SANTA CREU I SANT PAU   (Spain)

Author keywords

Association study; Calcium channel; Iron deficiency anaemia; Iron uptake; SNPs

Indexed keywords

CACNA2D3 PROTEIN; CALCIUM CHANNEL; FERRITIN; IRON; UNCLASSIFIED DRUG; CACNA2D3 PROTEIN, HUMAN; PROTEIN SUBUNIT;

ADULT; ALLELE; ARTICLE; CACNA2D3 GENE; FEMALE; GENE; GENE MAPPING; GENETIC ASSOCIATION; GENETIC RISK; GENETIC TRAIT; HETEROZYGOTE; HUMAN; IRON BLOOD LEVEL; IRON DEFICIENCY ANEMIA; IRON TRANSPORT; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SYSTEMATIC REVIEW (TOPIC); ADOLESCENT; BLOOD; CHEMISTRY; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; MEAN CORPUSCULAR VOLUME; METABOLISM; MIDDLE AGED; PHENOTYPE; PROTEIN SUBUNIT; YOUNG ADULT;

ADOLESCENT; ADULT; ALLELES; ANEMIA, IRON-DEFICIENCY; CALCIUM CHANNELS; ERYTHROCYTE INDICES; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; IRON; MIDDLE AGED; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN SUBUNITS; YOUNG ADULT;

EID: 84943563911     PISSN: 10799796     EISSN: 10960961     Source Type: Journal    
DOI: 10.1016/j.bcmd.2015.07.008     Document Type: Article

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