Nephrotic Syndrome: Novel Monogenic Causes of Galloway-Mowat Syndrome

Overview

Journal Nat Rev Nephrol

Specialty Nephrology

Date 2017 Sep 12

PMID 28890537

Citations 4

Authors

Ellen F Carney

Affiliations

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Citing Articles

Novel LAGE3 Pathogenic Variants Combined with TRPC6 and NUP160 Variants in Galloway-Mowat Syndrome: A Case Report.

Huang L, Zhang X, Zhang Y, Wang Y, Mao J Case Rep Nephrol Dial. 2023; 13(1):148-155.

PMID: 37900929 PMC: 10601869. DOI: 10.1159/000533580.

Conservation and Diversification of tRNA tA-Modifying Enzymes across the Three Domains of Life.

Su C, Jin M, Zhang W Int J Mol Sci. 2022; 23(21).

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L Antigen Family Member 3 Serves as a Prognostic Biomarker for the Clinical Outcome and Immune Infiltration in Skin Cutaneous Melanoma.

Song J, Jin C, Chen E, Dong X, Zhu L Biomed Res Int. 2021; 2021:6648182.

PMID: 33829062 PMC: 8000545. DOI: 10.1155/2021/6648182.

Nephrological and urological complications of homozygous c.974G>A (p.Arg325Gln) OSGEP mutations.

Wang P, Prasad C, Rodriguez Cuellar C, Filler G Pediatr Nephrol. 2018; 33(11):2201-2204.

PMID: 30141175 DOI: 10.1007/s00467-018-4060-x.

References

Braun D, Rao J, Mollet G, Schapiro D, Daugeron M, Tan W . Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Nat Genet. 2017; 49(10):1529-1538. PMC: 5819591. DOI: 10.1038/ng.3933. View