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Updated: Nov 17, 2025

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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SLCO2A1 gene is the causal gene for both primary hypertrophic osteoarthropathy and hereditary chronic enteropathy
Junji Umeno1, Takayuki Matsumoto2, Yuta Fuyuno1
1Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Fukuoka, Japan.
Journal of Orthopaedic Translation
|February 12, 2021
Abstract
No abstract available in PubMed .
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