ArticleMolecular genetics & genomic medicine2023

Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in Iran and literature review.

Fereshteh Jamshidi et al.PubMed ↗Full text ↗Publisher ↗

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