Associated Papers
Dual phenotypes in recurrent astrocytoma, IDH-mutant; coexistence of IDH-mutant and IDH-wildtype components: a case report with genetic and epigenetic analysis.
Yamaguchi J et al.
Acta Neuropathologica Communications, 2024
39456052 (PubMed )
Supplement: 40478_2024_1879_MOESM3_ESM.xlsx › NGY-R2A
Sézary syndrome originates from heavily mutated hematopoietic progenitors.
Harro CM et al.
Blood Advances, 2023
37531660 (PubMed )
Supplement: BLOODA_ADV-2022-008562-mmc1.pdf
Genetic landscape in coagulation factor XIII associated defects - Advances in coagulation and beyond.
Javed H et al.
Blood Reviews, 2023
Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A2.
Ivaškevičius V et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2017
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