Two novel variants of uncertain significance in GP9 associated with Bernard–Soulier syndrome: Are they true mutations?
Bernard–Soulier syndrome (BSS) is an autosomal recessive major thrombocytopathy, the symptoms of which are mainly marked by mucocutaneous bleeding. This rare disease, initially described in the 1970s, is the result of an abnormal formation of the glycoprotein complex Ib-IX-V (GP Ib-IX-V), a platelet...
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| Hoofdauteurs: | , , , , , , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Taylor & Francis Group
2018-04-01
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| Reeks: | Platelets |
| Onderwerpen: | |
| Online toegang: | http://dx.doi.org/10.1080/09537104.2017.1371288 |
| Tags: |
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