Found: 2
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Vanishing urate, acute kidney injury episodes and a homozygous SLC2A9 mutation.
- Published in:
- 2015
- By:
- Publication type:
- Letter
Familial Partial Lipodystrophy: Clinical Features, Genetics and Treatment in a Greek Referral Center.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 15, p. 12045, doi. 10.3390/ijms241512045
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- Publication type:
- Article