Double heterozygosity of the GPIIb gene in a Swiss patient with Glanzmann's thrombasthenia
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Do cell junction protein mutations cause an airway phenotype in mice or humans?Deep Vein Thrombosis, Raynaud's Phenomenon, and Prinzmetal Angina in a Patient with Glanzmann Thrombasthenia.Mapping the binding domains of the alpha(IIb) subunit. A study performed on the activated form of the platelet integrin alpha(IIb)beta(3).Mutations in the beta3 gene giving rise to type I Glanzmann thrombasthenia in two families in Portugal.
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Double heterozygosity of the GPIIb gene in a Swiss patient with Glanzmann's thrombasthenia
description
article
@en
im September 1998 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована у вересні 1998
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name
Double heterozygosity of the G ...... ith Glanzmann's thrombasthenia
@en
Double heterozygosity of the G ...... ith Glanzmann's thrombasthenia
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type
label
Double heterozygosity of the G ...... ith Glanzmann's thrombasthenia
@en
Double heterozygosity of the G ...... ith Glanzmann's thrombasthenia
@nl
prefLabel
Double heterozygosity of the G ...... ith Glanzmann's thrombasthenia
@en
Double heterozygosity of the G ...... ith Glanzmann's thrombasthenia
@nl
P2093
P2860
P1476
Double heterozygosity of the G ...... ith Glanzmann's thrombasthenia
@en
P2093
P2860
P304
P356
10.1046/J.1365-2141.1998.00852.X
P407
P577
1998-09-01T00:00:00Z