Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta

Journal of Dental Research

Volumn 87, Issue 12, 2008, Pages 1108-1111

  McKnight, D A ^a   Simmer, J P ^b   Hart, P S ^c   Hart, T C ^a   Fisher, L W ^a  

^a NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH   (United States)

^b UNIVERSITY OF MICHIGAN SCHOOL OF DENTISTRY   (United States)

^c NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

Dentin dysplasia; Dentinogenesis imperfecta; DPP; DSPP

Indexed keywords

ASPARTIC ACID; DSPP PROTEIN, HUMAN; PHOSPHOPROTEIN; SCLEROPROTEIN; SERINE; SIALOGLYCOPROTEIN; UNCLASSIFIED DRUG;

3' UNTRANSLATED REGION; AMINO ACID SEQUENCE; ARTICLE; BASE PAIRING; CHROMOSOME 4; EXON; FRAMESHIFT MUTATION; GENE DELETION; GENETICS; HAPLOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; NUCLEOTIDE REPEAT; PEDIGREE; PHENOTYPE; PROMOTER REGION; SEQUENCE ANALYSIS; TOOTH MALFORMATION;

3' UNTRANSLATED REGIONS; AMINO ACID SEQUENCE; ASPARTIC ACID; BASE PAIRING; CHROMOSOMES, HUMAN, PAIR 4; DENTIN DYSPLASIA; DENTINOGENESIS IMPERFECTA; EXONS; EXTRACELLULAR MATRIX PROTEINS; FRAMESHIFT MUTATION; HAPLOTYPES; HETEROZYGOTE; HOMOZYGOTE; HUMANS; PEDIGREE; PHENOTYPE; PHOSPHOPROTEINS; PROMOTER REGIONS, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; SEQUENCE ANALYSIS, PROTEIN; SEQUENCE DELETION; SERINE; SIALOGLYCOPROTEINS;

EID: 58149401847     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/154405910808701217     Document Type: Article

References (14)

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