Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary

Journal of Dental Research

Volumn 81, Issue 11, 2002, Pages 738-742

  Kida, M ^a   Ariga, T ^a   Shirakawa, T ^a   Oguchi, H ^a   Sakiyama, Y ^a  

^a HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ENAMEL PROTEIN; GUANOSINE; TUFTELIN;

AMELOGENESIS IMPERFECTA; ARTICLE; CHILD; CHROMOSOME 4; DOMINANT GENE; EXON; FEMALE; GENETICS; HUMAN; INTRON; MALE; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PEDIGREE; SINGLE STRAND CONFORMATION POLYMORPHISM; STOP CODON;

AMELOGENESIS IMPERFECTA; BASE SEQUENCE; CHILD; CHROMOSOMES, HUMAN, PAIR 4; CODON, NONSENSE; DENTAL ENAMEL PROTEINS; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENES, DOMINANT; GUANOSINE; HUMANS; INTRONS; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0036827621     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/0810738     Document Type: Article

References (19)