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
Molecular Genetics & Genomic Medicine（2023）
Key words
FGF3,Iran,LAMM syndrome,whole-exome sequencing
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