Associated Papers
Oro-dental phenotyping and report of three families with RELT-associated amelogenesis imperfecta.
Resende KKM et al.
European Journal of Human Genetics : Ejhg, 2023
New missense variants in RELT causing hypomineralised amelogenesis imperfecta.
Nikolopoulos G et al.
Clinical Genetics, 2020
ADAM10 is Expressed by Ameloblasts, Cleaves the RELT TNF Receptor Extracellular Domain and Facilitates Enamel Development.
Ikeda A et al.
Scientific Reports, 2019
Mutations in RELT cause autosomal recessive amelogenesis imperfecta.
Kim JW et al.
Clinical Genetics, 2019
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