A novel ADCK4 mutation in a Chinese family with ADCK4-Associated glomerulopathy
Author:
Funder
National Natural Science Foundation of China
Province Key Technology R&D Program
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference21 articles.
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3. A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation;Kurogouchi;Am. J. Nephrol.,1998
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5. Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiency;Desbats;J. Inherit. Metab. Dis.,2015
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