Glycoprotein Ib: Difference between revisions
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'''Glycoprotein Ib''', abbreviated to '''GPIb''' is a component of the GPIb-V-IX complex on [[platelets]]. It is deficient in the [[Bernard-Soulier syndrome]]. A gain-of-function mutation causes platelet-type [[von Willebrand's disease]]<ref>McPherson & Pincus: Henry's Clinical Diagnosis and Management by Laboratory Methods, 21st ed., pp. 760-2 (W.B. Saunders, 2006).</ref> | '''Glycoprotein Ib''', abbreviated to '''GPIb''' is a component of the GPIb-V-IX complex on [[platelets]]. It is deficient in the [[Bernard-Soulier syndrome]]. A gain-of-function mutation causes platelet-type [[von Willebrand's disease]]<ref>McPherson & Pincus: Henry's Clinical Diagnosis and Management by Laboratory Methods, 21st ed., pp. 760-2 (W.B. Saunders, 2006).</ref> | ||
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Latest revision as of 17:54, 4 September 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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Glycoprotein Ib, abbreviated to GPIb is a component of the GPIb-V-IX complex on platelets. It is deficient in the Bernard-Soulier syndrome. A gain-of-function mutation causes platelet-type von Willebrand's disease[1]
See also
References
- ↑ McPherson & Pincus: Henry's Clinical Diagnosis and Management by Laboratory Methods, 21st ed., pp. 760-2 (W.B. Saunders, 2006).