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Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop).
Simurda T, Caccia S, Asselta R, Zolkova J, Stasko J, Skornova I, Snahnicanova Z, Loderer D, Lasabova Z, Kubisz P. Simurda T, et al. Among authors: snahnicanova z. J Thromb Thrombolysis. 2020 Jul;50(1):233-236. doi: 10.1007/s11239-019-01991-x. J Thromb Thrombolysis. 2020. PMID: 31712947 Free article. No abstract available.
Association of Polymorphisms in CYBA, SOD1, and CAT Genes with Type 1 Diabetes and Diabetic Peripheral Neuropathy in Children and Adolescents.
Snahnicanova Z, Mendelova A, Grendar M, Holubekova V, Kostkova M, Pozorciakova K, Jancinová M, Kasubova I, Vojtkova J, Durdik P, Lasabova Z, Ciljakova M, Banovcin P. Snahnicanova Z, et al. Genet Test Mol Biomarkers. 2018 Jul;22(7):413-419. doi: 10.1089/gtmb.2018.0018. Epub 2018 Jun 20. Genet Test Mol Biomarkers. 2018. PMID: 29924645
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