Associated Papers
Whole-exome sequencing identifies ECPAS as a novel potentially pathogenic gene in multiple hereditary families with nonsyndromic orofacial cleft.
Zhao H et al.
Protein & Cell, 2024
38695759 (PubMed )
Supplement: pwae021_suppl_supplementary_figures_s1-s10_tables_s1-s2.pdf
Genetic variations in exon 10 of ENAM and their association with early childhood caries.
Sharma A et al.
Journal of Oral Biosciences, 2024
Prediction of Early Childhood Caries Based on Single Nucleotide Polymorphisms Using Neural Networks.
Zaorska K et al.
Genes, 2021
ENAM mutations and digenic inheritance.
Zhang H et al.
Molecular Genetics & Genomic Medicine, 2019
Association between ENAM polymorphisms and dental caries in children.
Devang Divakar D et al.
Saudi Journal of Biological Sciences, 2019
Dental caries and enamelin haplotype.
Chaussain C et al.
Journal of Dental Research, 2014
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeII_
Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.
Hart PS et al.
Archives of Oral Biology, 2003
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