A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family

BMC Medical Genetics

Volumn 11, Issue 1, 2010, Pages

  Bai, Haihua ^a,b   Agula, Hasi ^a   Wu, Qizhu ^b   Zhou, Wenyu ^c   Sun, Yujing ^c   Qi, Yue ^c   Latu, Suya ^b   Chen, Yujie ^b   Mutu, Jiri ^b   Qiu, Changchun ^c  

^a INNER MONGOLIA UNIVERSITY   (China)

^b INNER MONGOLIA UNIVERSITY FOR NATIONALITIES   (China)

^c INSTITUTE OF BASIC MEDICAL SCIENCES   (China)

Author keywords

[No Author keywords available]

Indexed keywords

DENTIN SIALOPHOSPHOPROTEIN; PROTEIN PRECURSOR; UNCLASSIFIED DRUG; PHOSPHOPROTEIN; SCLEROPROTEIN; SIALOGLYCOPROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; BONE MALFORMATION; CHINA; CLINICAL ARTICLE; CONTROLLED STUDY; DENTINOGENESIS IMPERFECTA TYPE II; DNA SEQUENCE; DNA SPLICING; EXON; FAMILY STUDY; FEMALE; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC RECOMBINATION; GENOTYPE; HAPLOTYPE; HEARING LOSS; HUMAN; HUMAN CELL; INTRON; LINKAGE ANALYSIS; MALE; MUTATIONAL ANALYSIS; PEDIGREE ANALYSIS; POLYMERASE CHAIN REACTION; TOOTH DISCOLORATION; TOOTH MALFORMATION; TOOTH PULP DISEASE; ASIAN; GENETICS; MONGOLIA; MUTATION; PEDIGREE; PHENOTYPE; RNA SPLICING;

ASIAN CONTINENTAL ANCESTRY GROUP; DENTINOGENESIS IMPERFECTA; EXTRACELLULAR MATRIX PROTEINS; FEMALE; HAPLOTYPES; HUMANS; MALE; MONGOLIA; MUTATION; PEDIGREE; PHENOTYPE; PHOSPHOPROTEINS; RNA SPLICING; SEQUENCE ANALYSIS, DNA; SIALOGLYCOPROTEINS; TOOTH ABNORMALITIES;

EID: 77649100985     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-11-23     Document Type: Article

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