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Clinical Exome Sequencing Identifies a Novel Mutation of the GREB1L Gene in a Chinese Family with Renal Agenesis.
Genetic Testing and Molecular Biomarkers ( IF 1.1 ) Pub Date : 2020-07-31 , DOI: 10.1089/gtmb.2020.0036
Ancong Wang 1, 2 , Baoju Ji 3 , Fengxia Wu 4 , Xiangyu Zhao 3, 5
Affiliation  

Background: Renal agenesis (RA) is one of the most severe congenital anomalies of the kidney and urinary tract; it is known to be highly genetically heterogeneous. The purpose of this study was to explore the clinical significance of genetic diagnostics in a Chinese RA family.
更新日期:2020-08-06
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