GATA2 deficiency syndrome: A decade of discovery

GATA2 deficiency syndrome (G2DS) is a rare autosomal dominant genetic disease predisposing to a range of symptoms, of which myeloid malignancy and immunodeficiency including recurrent infections are most common. In the last decade since it was first reported, there have been over 480 individuals ide...

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Detalles Bibliográficos
Autores principales: Homan, Claire C., Venugopal, Parvathy, Arts, Peer, Shahrin, Nur H., Feurstein, Simone, Rawlings, Lesley, Lawrence, David M., Andrews, James, King‐Smith, Sarah L., Harvey, Natasha L., Brown, Anna L., Scott, Hamish S., Hahn, Christopher N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Mutation Updates
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291163/
https://www.ncbi.nlm.nih.gov/pubmed/34387894
http://dx.doi.org/10.1002/humu.24271

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291163/
https://www.ncbi.nlm.nih.gov/pubmed/34387894
http://dx.doi.org/10.1002/humu.24271

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