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ArticleMolecular genetics & genomic medicine2025

A Novel Compound Heterozygous Variant in the ABHD12 Gene Cause PHARC Syndrome in a Chinese Family: The Proband Presenting New Genotype and Phenotype.

Meijiao Ma et al.PubMed ↗Full text ↗Publisher ↗

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2025
2026
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Full record →Abstract, authors, funding and every citing paper · PMID 39910854