RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease

Detalles Bibliográficos
Autores principales: Wontakal, Sandeep N., Britto, Mishan, Zhang, Huan, Han, Yongshuai, Gao, Chengjie, Tannenbaum, Sarah, Durham, Benjamin H., Lee, Margaret T., An, Xiuli, Mishima, Masanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2022
Materias:
Letters to Blood
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900277/
https://www.ncbi.nlm.nih.gov/pubmed/34818416
http://dx.doi.org/10.1182/blood.2021012334

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900277/
https://www.ncbi.nlm.nih.gov/pubmed/34818416
http://dx.doi.org/10.1182/blood.2021012334

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