Associated Papers
A Novel Missense Mutation in the FGF3 Gene of a Chinese Patient with LAMM Syndrome.
Zhang K et al.
Biochemical Genetics, 2025
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.
Jamshidi F et al.
Molecular Genetics & Genomic Medicine, 2023
LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations.
Sensi A et al.
American Journal of Medical Genetics. Part A, 2011
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