Articles with "cakut humans" as a keyword



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COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans

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Published in 2019 at "Human Genetics"

DOI: 10.1007/s00439-019-02042-4

Abstract: Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney disease (~ 45%) that manifests before 30 years of age. The genetic locus containing COL4A1 (13q33–34) has been implicated in… read more here.

Keywords: potential novel; cause; col4a1 mutations; cakut ... See more keywords