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).
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| Description | scientific article published on 16 November 2015 |
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author: Christoph Daniel Cécile Jeanpierre Alexandra Chadt Hadi Al-Hasani |
| Publication date | November 16, 2015 |
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