Associated Papers
[Molecular basis of primary renal hyperuricemia : role of the human urate transporter hURAT1].
Unger S et al.
Zeitschrift Fur Rheumatologie, 2007
Homozygous frameshift mutation in the SLC22A12 gene in a patient with primary gout and high levels of serum uric acid.
Vázquez-Mellado J et al.
Journal of Clinical Pathology, 2007
Molecular analysis of the SLC22A12 (URAT1) gene in patients with primary gout.
Vázquez-Mellado J et al.
Rheumatology (oxford, England), 2007
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