Absence of SLC22A12/URAT1 gene mutations in patients with primary gout

Journal of Rheumatology

Volumn 39, Issue 9, 2012, Pages 1901-

  Torres, Rosa J ^a   De Miguel, Eugenio ^a   Bailen, Rebeca ^a   Puig, Juan G ^a  

^a HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; ORGANIC CATION TRANSPORTER; ORGANIC CATION TRANSPORTER 1; PROTEIN URAT1; UNCLASSIFIED DRUG; URATE;

ADULT; COHORT ANALYSIS; DISEASE ASSOCIATION; DNA FLANKING REGION; DNA SEQUENCE; EXON; FEMALE; GENE; GENE AMPLIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GOUT; HUMAN; HYPOURICEMIA; INTRON; LETTER; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SLC22A12 GENE; URAT1 GENE; URIC ACID BLOOD LEVEL; URIC ACID URINE LEVEL;

AGED; FEMALE; GENETIC ASSOCIATION STUDIES; GOUT; HUMANS; MALE; MIDDLE AGED; MUTATION; ORGANIC ANION TRANSPORTERS; ORGANIC CATION TRANSPORT PROTEINS; SPAIN;

EID: 84865757349     PISSN: 0315162X     EISSN: 14992752     Source Type: Journal    
DOI: 10.3899/jrheum.120451     Document Type: Letter

References (10)

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