Cite
HARVARD Citation
Kawamura, Y. et al. (2020). Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families. Rheumatology. pp. 3988-3990. [Online].
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Kawamura, Y. et al. (2020). Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families. Rheumatology. pp. 3988-3990. [Online].