Novel ACTN1 variants in cases of thrombocytopenia

The ACTN1 gene has been implicated in inherited macrothrombocytopenia. To decipher the spectrum of variants and phenotype of ACTN1‐related thrombocytopenia, we sequenced the ACTN1 gene in 272 cases of unexplained chronic or familial thrombocytopenia. We identified 15 rare, monoallelic, nonsynonymous...

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Detalles Bibliográficos
Autores principales: Vincenot, Anne, Saultier, Paul, Kunishima, Shinji, Poggi, Marjorie, Hurtaud‐Roux, Marie‐Françoise, Roussel, Alain, ACTN1 study coinvestigators, Schlegel, Nicole, Alessi, Marie‐Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900141/
https://www.ncbi.nlm.nih.gov/pubmed/31237726
http://dx.doi.org/10.1002/humu.23840

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900141/
https://www.ncbi.nlm.nih.gov/pubmed/31237726
http://dx.doi.org/10.1002/humu.23840

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