A new frameshift mutation encoding a truncated amelogenin leads to X-linked amelogenesis imperfecta

Archives of Oral Biology

Volumn 47, Issue 3, 2002, Pages 211-217

  Greene, S R ^a   Yuan, Z A ^a   Wright, J T ^b   Amjad, H ^a   Abrams, W R ^a   Buchanan, J A ^a   Trachtenberg, D I ^c   Gibson, C W ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b UNIVERSITY OF NORTH CAROLINA   (United States)

^c NONE   (United States)

Author keywords

Amelogenesis imperfecta; Amelogenin; Enamel; Genetic disease

Indexed keywords

AMELOGENIN; AMELOGENINS; DNA; ENAMEL PROTEIN;

ADULT; AMELOGENESIS IMPERFECTA; AMINO ACID SEQUENCE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CHROMOSOME DELETION X; CLINICAL ARTICLE; DISEASE ASSOCIATION; DISEASE SEVERITY; DNA SEQUENCE; ENAMEL; FEMALE; FRAMESHIFT MUTATION; GENETIC LINKAGE; GENETICS; GENOTYPE; HUMAN; HYPOPLASIA; MALE; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; SEX CHROMOSOME ABERRATION; X CHROMOSOME; X CHROMOSOME LINKED DISORDER;

ADULT; AMELOGENESIS IMPERFECTA; AMELOGENIN; AMINO ACID SEQUENCE; DENTAL ENAMEL PROTEINS; DNA MUTATIONAL ANALYSIS; FEMALE; FRAMESHIFT MUTATION; GENOTYPE; HUMANS; LINKAGE (GENETICS); MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; SEX CHROMOSOME ABERRATIONS; X CHROMOSOME;

EID: 0036008478     PISSN: 00039969     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-9969(01)00111-X     Document Type: Article

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