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Correlation of Kidney Function, Volume and Imaging Findings, and PKHD1 Mutations in 73 Patients with Autosomal Recessive Polycystic Kidney Disease
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CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2010)
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International registry for primary Hyperoxaluria
JC Lieske et al.
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Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
M Zenker et al.
HUMAN MOLECULAR GENETICS (2004)
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