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Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)

Crossref DOI link: https://doi.org/10.1007/s00439-015-1610-1

Published Online: 2015-11-16

Published Print: 2016-01

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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