DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Valina MR, Larsen CP, Kanosky S, Suchy SF, Nield LS, Onder AM.
A novel CLCN5 mutation in a boy with asymptomatic proteinuria and focal global glomerulosclerosis.
Clin Nephrol 2013;
80 (05) 377-384
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