Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta

Authors

Tero T. Kivelä, University of Helsinki and Helsinki University Hospital, Finland
Walter Lisch, Johannes Gutenberg University Mainz, Germany
Jayne E. Weiss, LSU Health Sciences Center - New OrleansFollow

Document Type

Letter to the Editor

Publication Date

9-24-2024

Publication Title

Journal of Medical Genetics

PubMed ID

39214682

Recommended Citation

Kivelä, Tero T.; Lisch, Walter; and Weiss, Jayne E., "Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta" (2024). School of Medicine Faculty Publications. 2951.
https://digitalscholar.lsuhsc.edu/som_facpubs/2951
10.1136/jmg-2024-110310