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A mitochondrial DNA deletion presenting with corneal clouding and severe Fanconi syndrome.
Pediatr Nephrol. 2012 May;27(5):869-72. doi: 10.1007/s00467-011-2096-2. Epub 2012 Jan 20.
Pediatr Nephrol. 2012.
PMID: 22271366
Relationship of serum paraoxonase 1 activity and paraoxonase 1 genotype to risk of systemic lupus erythematosus.
Tripi LM, Manzi S, Chen Q, Kenney M, Shaw P, Kao A, Bontempo F, Kammerer C, Kamboh MI.
Tripi LM, et al.
Arthritis Rheum. 2006 Jun;54(6):1928-39. doi: 10.1002/art.21889.
Arthritis Rheum. 2006.
PMID: 16729301
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