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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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MYH9-related disease misdiagnosed for a decade: lessons from diagnostic pitfalls

S Okuyama1, T Ueki2, K Tanaka2

  • 1Department of Hematology, Yamagata Prefectural Central Hospital, 1800 Aoyagi, Yamagata-shi, Yamagata 990-2292, Japan.

QJM : Monthly Journal of the Association of Physicians
|April 24, 2024
PubMed
Abstract

No abstract available in PubMed .

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