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2023
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2019
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Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis.
Not available
S-EPMC6426152
|
biostudies-literature
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OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis.
Not available
S-EPMC9992313
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biostudies-literature
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Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
Not available
S-EPMC6115658
|
biostudies-literature
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