High-Throughput Splicing Assays Identify Known and Novel WT1 Exon 9 Variants in Nephrotic Syndrome.

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Bibliographic Details
Title: High-Throughput Splicing Assays Identify Known and Novel WT1 Exon 9 Variants in Nephrotic Syndrome.
Authors: Smith C; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, USA.; Department of Computational Medicine and Bioinformatics, University of Michigan Medical School, Ann Arbor, Michigan, USA., Burugula BB; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, USA., Dunn I; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, USA., Aradhya S; Invitae, San Francisco, California, USA., Kitzman JO; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, USA.; Department of Computational Medicine and Bioinformatics, University of Michigan Medical School, Ann Arbor, Michigan, USA., Yee JL; Department of Pediatrics, Division of Nephrology, University of Michigan, Ann Arbor, Michigan, USA.
Source: Kidney international reports [Kidney Int Rep] 2023 Aug 05; Vol. 8 (10), pp. 2117-2125. Date of Electronic Publication: 2023 Aug 05 (Print Publication: 2023).
Publication Type: Journal Article
Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 101684752 Publication Model: eCollection Cited Medium: Internet ISSN: 2468-0249 (Electronic) Linking ISSN: 24680249 NLM ISO Abbreviation: Kidney Int Rep Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2468-0249
DOI:10.1016/j.ekir.2023.07.033