Heterozygous mutation in SLC36A2 gene causing hyperglycinuria and nephrolithiasis
Background: Childhood nephrolithiasis cases reported worldwide has been increasing over the last decade. The majority of cases reported are related to calcium oxalate formation which results in impairment of glycine transport in the renal tubule leading to hyperglycinuria and impaired urinary oxalat...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Discover STM Publishing Ltd
2019-06-01
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| Series: | Journal of Biochemical and Clinical Genetics |
| Subjects: | |
| Online Access: | http://www.ejmanager.com/fulltextpdf.php?mno=17746 |