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- W2015379860 abstract "Summary. Glanzmann's thrombasthenia (GT) is a hereditary bleeding disorder caused by a quantitative or qualitative defect in the integrin α IIb β 3 . A new mutation, a T to C substitution at base 258 in the α IIb gene, leading to the replacement of Leu 55 with Pro, was found by sequence analysis of a patient's α IIb cDNA. In transfection experiments using COS7 cells, the cells co‐transfected with the mutated α IIb cDNA containing C 258 and wild‐type β 3 cDNA scarcely expressed the α IIb β 3 complex. The Leu 55 to Pro substitution in the α IIb gene was found to be responsible for this case of Glanzmann's thrombasthenia." @default.
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- W2015379860 date "2002-08-15" @default.
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- W2015379860 title "A Leu<sup>55</sup> to Pro substitution in the integrin α<sub>IIb</sub> is responsible for a case of Glanzmann's thrombasthenia" @default.
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- W2015379860 doi "https://doi.org/10.1046/j.1365-2141.2002.03678.x" @default.
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