Connection
Christopher Ng to Mutation
This is a "connection" page, showing publications Christopher Ng has written about Mutation.
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Koukouritaki SB, Thinn AMM, Ashworth KJ, Fang J, Slater HS, Du LM, Nguyen HTT, Pillois X, Nurden AT, Ng CJ, Di Paola J, Zhu J, Wilcox DA. A single F153S?3 mutation causes constitutive integrin aIIb?3 activation in a variant form of Glanzmann thrombasthenia. Blood Adv. 2023 07 11; 7(13):3180-3191.
Score: 0.024
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White-Adams TC, Ng CJ, Jacobi PM, Haberichter SL, Di Paola JA. Mutations in the D'D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF. Thromb Res. 2016 Sep; 145:112-8.
Score: 0.015