Kidney International
Homozygous mutations found in patients with hereditary nephritis, sensorineural deafness and epidermolysis bullosa (MIM#609057) Cd151-null mice develop proteinutira, glomerulosclerosis and other renal defects 27,28 CDC5L A patient with bilateral multicystic renal dysplasia has a breakpoint translocation in CDC5L 29 CDH1 ................
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