Associated Papers
Proteomic subtypes enrich current acute myeloid leukemia nomenclature and reflect intrinsic pathogenesis alongside aging.
Cheng WY et al.
Blood, 2025
40829168 (PubMed )
Supplement: BLOOD_BLD-2024-027692-mmc5.xlsx › Sheet_1
Methylmalonic acidemia with homocystinuria in acute myeloid leukemia: a case report.
Cheng Y et al.
Bmc Pediatrics, 2025
Case Report: Neonatal nephropathy with polycystic appearance in child harboring WT1 variant.
Nguyen TTT et al.
Frontiers in Pediatrics, 2025
41450889 (PubMed )
Supplement: Presentation1.pdf
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 in WT1 Exon 8 to 9 Missense Variants.
Nagano C et al.
Kidney International Reports, 2021
34386660 (PubMed )
Supplement: mmc1.pdf
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