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Keyword:
Missense mutation
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MYH7 mutation in a pedigree with familial dilated hypertrophic cardiomyopathy: A case report and review of literature
1/21/2025 7:29:06 AM |
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Novel mutations of the Alström syndrome 1 gene in an infant with dilated cardiomyopathy: A case report
3/2/2022 4:52:53 AM |
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