Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations

Archives of Oral Biology

Volumn 47, Issue 4, 2002, Pages 261-265

  Hart, P S ^a   Aldred, M J ^b   Crawford, P J M ^c   Wright, N J ^d   Hart, T C ^a   Wright, J T ^e  

^a UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^b ROYAL CHILDREN'S HOSPITAL   (Australia)

^c UNIVERSITY OF BRISTOL   (United Kingdom)

^d UNIVERSITY OF QUEENSLAND   (Australia)

^e UNIVERSITY OF NORTH CAROLINA   (United States)

Author keywords

Amelogenesis; Amelogenin; Enamel; Hereditary; Hypoplasia; Mineralization

Indexed keywords

AMELOGENIN; AMELOGENINS; ENAMEL PROTEIN; HISTIDINE; LEUCINE; AMELX PROTEIN, HUMAN;

AMELOGENESIS IMPERFECTA; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; BASE PAIRING; CARBOXY TERMINAL SEQUENCE; CHEMISTRY; ENAMEL; EXON; FEMALE; FRAMESHIFT MUTATION; GENE AMPLIFICATION; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; GENETICS; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPOPLASIA; MALE; MINERALIZATION; MISSENSE MUTATION; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE; PHENOTYPE; PROTEIN TERTIARY STRUCTURE; SEX CHROMOSOME ABERRATION; STOP CODON; X CHROMOSOME; X CHROMOSOME LINKED DISORDER;

AMELOGENESIS IMPERFECTA; AMELOGENIN; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; CODON, NONSENSE; DENTAL ENAMEL PROTEINS; DNA MUTATIONAL ANALYSIS; FEMALE; FRAMESHIFT MUTATION; GENOTYPE; HISTIDINE; HUMANS; LEUCINE; LINKAGE (GENETICS); MALE; MUTATION, MISSENSE; PEDIGREE; PHENOTYPE; PROTEIN STRUCTURE, TERTIARY; SEX CHROMOSOME ABERRATIONS; X CHROMOSOME;

EID: 0036010022     PISSN: 00039969     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-9969(02)00003-1     Document Type: Article

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