ANKRD26 Gene Variant of Uncertain Significance in a Patient With Acute Myeloid Leukemia

ANKRD26-related thrombocytopenia is a rare inherited disorder associated with an increased risk of malignancy. While the genetic mutations underlying this condition are well understood, there is limited knowledge regarding its contribution to myeloid neoplasms, such as acute myeloid leukemia (AML)....

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Detalles Bibliográficos
Autores principales: McCormick, Benjamin J, Chirila, Razvan M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101738/
https://www.ncbi.nlm.nih.gov/pubmed/37065357
http://dx.doi.org/10.7759/cureus.36152

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101738/
https://www.ncbi.nlm.nih.gov/pubmed/37065357
http://dx.doi.org/10.7759/cureus.36152

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