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Inherited thrombocytopenias: the beat goes on
In this issue of Blood, Bottega et al document mutations in ACTN1, which encodes the cytoskeletal protein α-actinin 1, in 10 of 239 consecutive probands with an inherited thrombocytopenia—making ACTN1 an important cause of familial thrombocytopenia.(1)
Bewaard in:
| Gepubliceerd in: | Blood |
|---|---|
| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Society of Hematology
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4311225/ https://ncbi.nlm.nih.gov/pubmed/25634615 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2014-11-610675 |
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