Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele

Detalles Bibliográficos
Autores principales: Sakurai, M, Kasahara, H, Yoshida, K, Yoshimi, A, Kunimoto, H, Watanabe, N, Shiraishi, Y, Chiba, K, Tanaka, H, Harada, Y, Harada, H, Kawakita, T, Kurokawa, M, Miyano, S, Takahashi, S, Ogawa, S, Okamoto, S, Nakajima, H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771963/
https://www.ncbi.nlm.nih.gov/pubmed/26849013
http://dx.doi.org/10.1038/bcj.2015.81

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771963/
https://www.ncbi.nlm.nih.gov/pubmed/26849013
http://dx.doi.org/10.1038/bcj.2015.81

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