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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:
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
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author Wontakal, Sandeep N.
Britto, Mishan
Zhang, Huan
Han, Yongshuai
Gao, Chengjie
Tannenbaum, Sarah
Durham, Benjamin H.
Lee, Margaret T.
An, Xiuli
Mishima, Masanori
author_facet Wontakal, Sandeep N.
Britto, Mishan
Zhang, Huan
Han, Yongshuai
Gao, Chengjie
Tannenbaum, Sarah
Durham, Benjamin H.
Lee, Margaret T.
An, Xiuli
Mishima, Masanori
author_sort Wontakal, Sandeep N.
collection PubMed
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spelling pubmed-89002772022-03-07 RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease Wontakal, Sandeep N. Britto, Mishan Zhang, Huan Han, Yongshuai Gao, Chengjie Tannenbaum, Sarah Durham, Benjamin H. Lee, Margaret T. An, Xiuli Mishima, Masanori Blood Letters to Blood American Society of Hematology 2022-03-03 /pmc/articles/PMC8900277/ /pubmed/34818416 http://dx.doi.org/10.1182/blood.2021012334 Text en © 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.
spellingShingle Letters to Blood
Wontakal, Sandeep N.
Britto, Mishan
Zhang, Huan
Han, Yongshuai
Gao, Chengjie
Tannenbaum, Sarah
Durham, Benjamin H.
Lee, Margaret T.
An, Xiuli
Mishima, Masanori
RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease
title RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease
title_full RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease
title_fullStr RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease
title_full_unstemmed RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease
title_short RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease
title_sort racgap1 variants in a sporadic case of cda iii implicate the dysfunction of centralspindlin as the basis of the disease
topic Letters to Blood
url 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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