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- DOI: 10.1093/ndt/gfm311
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Molecular characterization of two patients with severe LCAT deficiency.
Charlton-Menys V, Pisciotta L, Durrington PN, Neary R, Short CC, Calabresi L, Calandra S, Bertolini S
Nephrol Dial Transplant. 2007;22( 8).
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Full-text held externally
- DOI: 10.1093/ndt/gfm311
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Adult; Female; Humans; Male; Microscopy, Electron; Mutation; blood: Aryldialkylphosphatase; diagnosis: Kidney Diseases; diagnosis: Lecithin Acyltransferase Deficiency; genetics: Corneal Diseases; metabolism: Lipoproteins; metabolism: Lipoproteins, HDL