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Updated: Jul 4, 2025

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Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
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Analysis of Hereditary FXII Deficiency Caused by Three Mutations Including a Novel Mutation
Longying Ye1, Meina Liu1, Lihong Yang1
1The First Affiliated Hospital of Wenzhou Medical University, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, Department of Clinical Laboratory, Wenzhou, China
Abstract
No abstract available in PubMed .
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