HeterozygousCOL17A1variants are a frequent cause of amelogenesis imperfecta
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Published:2024-08-30
Issue:
Volume:
Page:jmg-2024-110310
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ISSN:0022-2593
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Container-title:Journal of Medical Genetics
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language:en
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Short-container-title:J Med Genet
Author:
Kivelä Tero TORCID,
Lisch Walter,
Weiss Jayne E