Mingshan Wang
3PUBLICATIONS
7CO-AUTHORS
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Publications (3)
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|Feb 01, 2024
Analysis of Hereditary FXII Deficiency Caused by Three Mutations Including a Novel MutationLongying Ye, Meina Liu, Lihong Yang
|Dec 05, 2023
Genetic Analysis of Prekallikrein Deficiency in a Consanguineously Married Chinese Family.Yuan Chen, Meina Liu, Mingshan Wang
|Oct 21, 2022
Analysis of phenotype and gene mutation in three pedigrees with inherited antithrombin deficiency.Min Li, Shuting Jiang, Siqi Liu
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