(2025). Detection of a Novel Homozygous PEX5 Stop-Loss Variant Associated with Zellweger Syndrome in a Highly Endogamic Family. Application of Clinical Genetics.
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Chicago Style (17th ed.) Citation
"Detection of a Novel Homozygous PEX5 Stop-Loss Variant Associated with Zellweger Syndrome in a Highly Endogamic Family."
Application of Clinical Genetics 2025.
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MLA (9th ed.) Citation
"Detection of a Novel Homozygous PEX5 Stop-Loss Variant Associated with Zellweger Syndrome in a Highly Endogamic Family."
Application of Clinical Genetics, 2025.
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Warning: These citations may not always be 100% accurate.