Trp207Gly in platelet glycoprotein Ibalpha is a novel mutation that disrupts the connection between the leucine-rich repeat domain and the disulfide loop structure and causes Bernard-Soulier syndrome (Q33373167)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Trp207Gly in platelet glycoprotein Ibalpha is a novel mutation that disrupts the connection between the leucine-rich repeat domain and the disulfide loop structure and causes Bernard-Soulier syndrome |
scientific article |
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Trp207Gly in platelet glycoprotein Ibalpha is a novel mutation that disrupts the connection between the leucine-rich repeat domain and the disulfide loop structure and causes Bernard-Soulier syndrome (English)
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Seligsohn U
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Rosenberg N
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Lalezari S
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Landau M
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Shenkman B
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Izraeli S
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2 November 2006
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378-386
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