(2026). Identification of the MYH6 c.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family. Molecular Genetics & Genomic Medicine.
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Chicago Style (17th ed.) Citation
"Identification of the MYH6 C.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family."
Molecular Genetics & Genomic Medicine 2026.
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MLA (9th ed.) Citation
"Identification of the MYH6 C.804G>C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family."
Molecular Genetics & Genomic Medicine, 2026.
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Warning: These citations may not always be 100% accurate.