Associated Papers
High-Throughput Splicing Assays Identify Known and Novel WT1 Exon 9 Variants in Nephrotic Syndrome.
Smith C et al.
Kidney International Reports, 2023
37850022 (PubMed )
Supplement: mmc1.pdf
Genotype-phenotype correlation of WT1 mutation-related nephropathy in Chinese children.
Chen H et al.
Frontiers in Pediatrics, 2023
Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants.
Nagano C et al.
Kidney International Reports, 2021
34386660 (PubMed )
Supplement: mmc1.pdf
Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia.
Madan V et al.
Leukemia, 2016
27063598 (PubMed )
Supplement: leu201669x7.xls › Sheet_1
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