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Article

Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta.

Journal of medical genetics - 24 Sept 2024

Kivelä Tero T, Lisch Walter, Weiss Jayne E

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Share to Amelogenesis Imperfecta
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Share to Collagen Type XVII
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 39214682
DOI: 10.1136/jmg-2024-110310

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