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Analysis of disease-causing GATA1 mutations in murine gene complementation systems

Missense mutations in transcription factor GATA1 underlie a spectrum of congenital red blood cell and platelet disorders. We investigated how these alterations cause distinct clinical phenotypes by combining structural, biochemical, and genomic approaches with gene complementation systems that exami...

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Detalhes bibliográficos
Main Authors: Campbell, Amy E., Wilkinson-White, Lorna, Mackay, Joel P., Matthews, Jacqueline M., Blobel, Gerd A.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3695365/
https://ncbi.nlm.nih.gov/pubmed/23704091
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-03-488080
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