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LCAT deficiency, a rare inherited disorder associated with rapidly progressive kidney disease: genetic and phenotypic heterogeneity, pathogenesis of renal damage and therapeutic developments
Project
Academic Signature
Overview
Publications
Academic Signature
Il servizio di classificazione ACADEMIC SIGNATURE รจ IN BETA TESTING e i risultati potrebbero non essere corretti
Academic Signature (2)
Genetic Heterogeneity
Genetic Variation
Lecithin Cholesterol Acyltransferase Deficiency
Hypoalphalipoproteinemias
Overview
Type
CAR_RIC - Bandi Fondazione Cariplo
Funder
FONDAZIONE CARIPLO
External Organization
Funding Organization
Date/time interval
January 1, 2012 - December 31, 2013
Project duration
24 months
Publications
Outputs
Progression of chronic kidney disease in Familial LCAT Deficiency: a follow-up of the Italian cohort
JOURNAL OF LIPID RESEARCH
AMERICAN SOCIETY FOR BIOCHEMISTRY AND MOLECULAR BIOLOGY
2020
Academic Article
Open Access
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