Abstract
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
Original language | English (US) |
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Pages (from-to) | 748-750 |
Number of pages | 3 |
Journal | Blood |
Volume | 125 |
Issue number | 5 |
DOIs |
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State | Published - Jan 29 2015 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Immunology
- Hematology
- Cell Biology