Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta

Human Molecular Genetics

Volumn 10, Issue 16, 2001, Pages 1673-1677

  Rajpar, M Helen ^a   Harley, Kathryn ^b   Laing, Chris ^c   Davies, Robin M ^d   Dixon, Michael J ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b EDINBURGH DENTAL INSTITUTE   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d Dental Health Unit   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMELOGENIN; ENAMEL PROTEIN; ENAMELIN; RNA; UNCLASSIFIED DRUG;

AMELOGENESIS IMPERFECTA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 4Q; CHROMOSOME MAP; CLINICAL ARTICLE; CLINICAL GENETICS; CONTROLLED STUDY; DISEASE CLASSIFICATION; ENAMEL; FAMILY STUDY; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; GENETIC HETEROGENEITY; HUMAN; INTRON; MALE; MOLECULAR GENETICS; PHENOTYPE; PRIORITY JOURNAL; RNA SPLICING; TOOTH DEVELOPMENT; X CHROMOSOME RECESSIVE INHERITANCE;

EID: 0035422249     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.16.1673     Document Type: Article

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