Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia

Detalles Bibliográficos
Autores principales: Böckelmann, Lukas Clemens, Basu, Titiksha, Gründer, Albert, Wang, Wei, Breucker, Jan, Kaiser, Sandra, Pichler, Andrea, Pahl, Heike Luise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2021
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018143/
https://www.ncbi.nlm.nih.gov/pubmed/32554556
http://dx.doi.org/10.3324/haematol.2020.246587

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018143/
https://www.ncbi.nlm.nih.gov/pubmed/32554556
http://dx.doi.org/10.3324/haematol.2020.246587

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