The Possible Non-Mutational Causes of FVIII Deficiency: Non-Coding RNAs and Acquired Hemophilia A

Hemophilia type A (HA) is the most common type of blood coagulation disorder. While the vast majority of cases are inherited and caused by mutations in the F8 gene, recent data raises new questions regarding the non-heritability of this disease, as well as how other molecular mechanisms might lead t...

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Detalles Bibliográficos
Autores principales: Zimta, Alina-Andreea, Hotea, Ionut, Brinza, Melen, Blag, Cristina, Iluta, Sabina, Constantinescu, Catalin, Bashimov, Atamyrat, Marchis-Hund, Elisabeth-Antonia, Coudsy, Alexandra, Muller-Mohnssen, Laetitia, Dirzu, Noemi, Gulei, Diana, Dima, Delia, Serban, Margit, Coriu, Daniel, Tomuleasa, Ciprian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099106/
https://www.ncbi.nlm.nih.gov/pubmed/33968959
http://dx.doi.org/10.3389/fmed.2021.654197

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099106/
https://www.ncbi.nlm.nih.gov/pubmed/33968959
http://dx.doi.org/10.3389/fmed.2021.654197

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