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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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==References==
==References==
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[[Category:Proteins]]
[[Category:Proteins]]

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

  1. McPherson & Pincus: Henry's Clinical Diagnosis and Management by Laboratory Methods, 21st ed., pp. 760-2 (W.B. Saunders, 2006).

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