Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation

Journal of Dental Research

Volumn 79, Issue 7, 2000, Pages 1476-1481

  Ravassipour, D B ^a   Hart, P S ^c   Hart, T C ^c   Ritter, A V ^a   Yamauchi, M ^a   Gibson, C ^b   Wright, J T ^a  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c WAKE FOREST SCHOOL OF MEDICINE   (United States)

Author keywords

Amelogenesis imperfecta; Amelogenin; Dental; Enamel; Genetics; Immunolocalization; Ultrastructure

Indexed keywords

AMELOGENIN; AMELX PROTEIN, HUMAN; ENAMEL PROTEIN;

AMELOGENESIS IMPERFECTA; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; ENAMEL; FEMALE; GENETICS; HUMAN; IMMUNOPHENOTYPING; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; POINT MUTATION; ULTRASTRUCTURE;

AMELOGENESIS IMPERFECTA; AMELOGENIN; AMINO ACID SUBSTITUTION; CHILD; DENTAL ENAMEL; DENTAL ENAMEL PROTEINS; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; IMMUNOPHENOTYPING; MALE; MUTATION, MISSENSE; PEDIGREE; POINT MUTATION;

EID: 0034444658     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/00220345000790070801     Document Type: Article

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