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Article

Arg913Gln variation of SLC12A3 gene is associated with diabetic nephropathy in type 2 diabetes and Gitelman syndrome: a systematic review.

BMC nephrology - 28 Oct 2019

De la Cruz-Cano Eduardo, Jiménez-González Cristina Del C, Morales-García Vicente, Pineda-Pérez Conny, Tejas-Juárez Juan G, Rendón-Gandarilla Francisco J, Jiménez-Morales Silvia, Díaz-Gandarilla José A

Abstract excerpt

BACKGROUND: Diabetic nephropathy is a global common cause of chronic kidney disease and end-stage renal disease. A lot of research has been conducted in biomedical sciences, which has enhanced understanding of the pathophysiology of diabetic nephropathy and has expanded the potential available therapies. An increasing number of evidence suggests that genetic alterations play a major role in development and...

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Share to Diabetes Mellitus, Type 2
Share to Diabetic Nephropathies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Gitelman Syndrome

Share to Kidney Failure, Chronic

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Share to Sodium Chloride Symporters

Share to Solute Carrier Family 12, Member 3

Source

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Identifiers

PMID: 31660880
DOI: 10.1186/s12882-019-1590-9
PMCID: PMC6819471

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