Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta | Journal of Medical Genetics

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Genotype-phenotype correlations

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Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta

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Cite this article as:: Hany U, Watson CM, Liu L, et al

Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta

Journal of Medical Genetics Published Online First: 18 November 2023. doi: 10.1136/jmg-2023-109510