טוען...
Progression of chronic kidney disease in familial LCAT deficiency: a follow-up of the Italian cohort
Familial LCAT deficiency (FLD) is a rare genetic disorder of HDL metabolism, caused by loss-of-function mutations in the LCAT gene and characterized by a variety of symptoms including corneal opacities and kidney failure. Renal disease represents the leading cause of morbidity and mortality in FLD c...
שמור ב:
| הוצא לאור ב: | J Lipid Res |
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| Main Authors: | , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
The American Society for Biochemistry and Molecular Biology
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7707181/ https://ncbi.nlm.nih.gov/pubmed/32998975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1194/jlr.P120000976 |
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