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http://purl.uniprot.org/citations/25143514http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/25143514http://www.w3.org/2000/01/rdf-schema#comment"Amelogenesis imperfecta (AI) is a genetic disease affecting tooth enamel formation. AI can be an isolated entity or a phenotype of syndromes. To date, more than 10 genes have been associated with various forms of AI. We have identified 2 unrelated Turkish families with hypoplastic AI and performed mutational analysis. Whole-exome sequencing identified 2 novel heterozygous nonsense mutations in the ENAM gene (c.454G>T p.Glu152* in family 1, c.358C>T p.Gln120* in family 2) in the probands. Affected individuals were heterozygous for the mutation in each family. Segregation analysis within each family revealed individuals with incomplete penetrance or extremely mild enamel phenotype, in spite of having the same mutation with the other affected individuals. We believe that these findings will broaden our understanding of the clinical phenotype of AI caused by ENAM mutations."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.org/dc/terms/identifier"doi:10.1177/0022034514548222"xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/author"Kim J.W."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/author"Lee K.E."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/author"Lee Z.H."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/author"Bayram M."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/author"Gencay K."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/author"Seymen F."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/author"Tuna E.B."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/author"Koruyucu M."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/date"2014"xsd:gYear
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/name"J Dent Res"xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/pages"988-992"xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/title"ENAM mutations with incomplete penetrance."xsd:string
http://purl.uniprot.org/citations/25143514http://purl.uniprot.org/core/volume"93"xsd:string
http://purl.uniprot.org/citations/25143514http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/25143514
http://purl.uniprot.org/citations/25143514http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/25143514
http://purl.uniprot.org/uniprot/#_L8E8W5-mappedCitation-25143514http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/25143514
http://purl.uniprot.org/uniprot/#_Q8IWP4-mappedCitation-25143514http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/25143514
http://purl.uniprot.org/uniprot/#_Q8NFB4-mappedCitation-25143514http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/25143514
http://purl.uniprot.org/uniprot/#_Q9NRM1-mappedCitation-25143514http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/25143514
http://purl.uniprot.org/uniprot/Q9NRM1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/25143514
http://purl.uniprot.org/uniprot/Q8NFB4http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/25143514
http://purl.uniprot.org/uniprot/L8E8W5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/25143514