Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's disease

Movement Disorders

Volumn 17, Issue 6, 2002, Pages 1302-1304

  Lee, Pauline L ^a   Gelbert, Terri ^a   West, Carol ^a   Halloran, Carol ^a   Sipe, Jack C ^a   Beutler, Ernest ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

Iron responsive binding protein; IRP2; Parkinson's disease; Polymorphisms; SNPs

Indexed keywords

IRON; IRON REGULATORY FACTOR; ISOLEUCINE; LEUCINE; PHENYLALANINE; THREONINE; VALINE;

ADULT; ALLELE; AMINO ACID SUBSTITUTION; ANAMNESIS; ARTICLE; BIOACCUMULATION; BRAIN REGION; CAUCASIAN; CONTROLLED STUDY; DISEASE PREDISPOSITION; DNA POLYMORPHISM; FAMILIAL DISEASE; FAMILY HISTORY; FATHER; GENE DELETION; GENE FREQUENCY; GENE SEQUENCE; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; NEGRO; NERVE DEGENERATION; NUCLEOTIDE SEQUENCE; PARKINSON DISEASE; PREVALENCE; PRIORITY JOURNAL;

AFRICAN CONTINENTAL ANCESTRY GROUP; AGED; ALLELES; CHROMOSOMES, HUMAN, PAIR 15; DNA MUTATIONAL ANALYSIS; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXONS; FEMALE; GENE FREQUENCY; GENETICS, POPULATION; HETEROZYGOTE DETECTION; HUMANS; IRON REGULATORY PROTEIN 2; MALE; MIDDLE AGED; PARKINSON DISEASE; POLYMORPHISM, GENETIC; SEQUENCE ANALYSIS, DNA;

EID: 0036869157     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/mds.10253     Document Type: Article

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