Altered enamelin phosphorylation site causes amelogenesis imperfecta

Journal of Dental Research

Volumn 89, Issue 7, 2010, Pages 695-699

  Chan, H C ^a   Mai, L ^a   Oikonomopoulou, A ^a   Chan, H L ^a   Richardson, A S ^a   Wang, S K ^a   Simmer, J P ^a   Hu, J C C ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

Amelogenesis imperfecta; Enamel; Inherited diseases; Mutations; Tooth

Indexed keywords

ADENINE; CALCIUM; CASEIN KINASE; CYTOSINE; ENAMEL PROTEIN; GUANINE; LEUCINE; SERINE; THYMINE; TUFTELIN;

ADULT; ALLELE; AMELOGENESIS IMPERFECTA; AMINO ACID SEQUENCE; ARTICLE; CASE REPORT; ENAMEL HYPOPLASIA; EXON; FRAMESHIFT MUTATION; GENE DELETION; GENE EXPRESSION REGULATION; GENETICS; GOLGI COMPLEX; HUMAN; MALE; METABOLISM; MISSENSE MUTATION; PEDIGREE; PHOSPHORYLATION;

ADENINE; ALLELES; AMELOGENESIS IMPERFECTA; AMINO ACID SEQUENCE; CALCIUM; CASEIN KINASES; CYTOSINE; DENTAL ENAMEL HYPOPLASIA; DENTAL ENAMEL PROTEINS; EXONS; FRAMESHIFT MUTATION; GOLGI APPARATUS; GUANINE; HUMANS; LEUCINE; MALE; MUTAGENESIS, INSERTIONAL; MUTATION, MISSENSE; PEDIGREE; PHOSPHORYLATION; SEQUENCE DELETION; SERINE; THYMINE; YOUNG ADULT;

EID: 77953775520     PISSN: 00220345     EISSN: 15440591     Source Type: Journal    
DOI: 10.1177/0022034510365662     Document Type: Article

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