Common polymorphisms in the solute carrier SLC30A10 are associated with blood manganese and neurological function

Toxicological Sciences

Volumn 149, Issue 2, 2016, Pages 473-483

  Wahlberg, Karin ^a   Kippler, Maria ^b   Alhamdow, Ayman ^a   Rahman, Syed Moshfiqur ^b,c   Smith, Donald R ^d   Vahter, Marie ^b   Lucchini, Roberto G ^d,e,f   Broberg, Karin ^a,b  

^a LUND UNIVERSITY   (Sweden)

^b KAROLINSKA INSTITUTE   (Sweden)

^c INTERNATIONAL CENTRE FOR DIARRHOEAL DISEASE RESEARCH   (Bangladesh)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF BRESCIA   (Italy)

Author keywords

Blood Mn concentrations; Manganese exposure; Manganese neurotoxicity; Manganese regulation; Parkinsonism; SLC30A10

Indexed keywords

BIOLOGICAL MARKER; FERRITIN; MANGANESE; SLC30A10 PROTEIN; UNCLASSIFIED DRUG; CATION TRANSPORT PROTEIN; SLC30A8 PROTEIN, HUMAN; ZINC;

ADULT; ARGENTINA; ARTICLE; ATOMIC ABSORPTION SPECTROMETRY; BANGLADESH; BRAIN FUNCTION; FEMALE; FERRITIN BLOOD LEVEL; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC CODE; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; ITALY; MAJOR CLINICAL STUDY; MALE; MANGANESE BLOOD LEVEL; NEUROTOXICITY; PROTEIN EXPRESSION; SINGLE NUCLEOTIDE POLYMORPHISM; VELOCITY; AGED; ALLELE; BLOOD; GENETICS; NEUROTOXICITY SYNDROMES; STATISTICAL MODEL;

AGED; ALLELES; CATION TRANSPORT PROTEINS; FEMALE; GENOTYPE; HETEROZYGOTE; HUMANS; LINEAR MODELS; MALE; MANGANESE; NEUROTOXICITY SYNDROMES; POLYMORPHISM, SINGLE NUCLEOTIDE; ZINC;

EID: 84960097435     PISSN: 10966080     EISSN: 10960929     Source Type: Journal    
DOI: 10.1093/toxsci/kfv252     Document Type: Article

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