A novel DSPP mutation is associated with type II dentinogenesis Imperfecta in a chinese family

BMC Medical Genetics

Volumn 8, Issue , 2007, Pages

  Zhang, Xianqin ^a,c   Chen, Lanying ^b   Liu, Jingyu ^a   Zhao, Zhen ^b   Qu, Erjun ^b   Wang, Xiaotao ^b   Chang, Wei ^a   Xu, Chengqi ^a   Wang, Qing K ^a,c   Liu, Mugen ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b Henan University of Urban Construction   (China)

^c CLEVELAND CLINIC LERNER COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; PHOSPHOPROTEIN; PROLINE; SERINE; SIALOPHOSPHOPROTEIN; UNCLASSIFIED DRUG; DSPP PROTEIN, HUMAN; PRIMER DNA; SCLEROPROTEIN;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CHINESE; CHROMOSOME 4Q; CLINICAL ARTICLE; CONTROLLED STUDY; DENTIN; DNA SEQUENCE; EXON; FEMALE; GENE MUTATION; HETEROZYGOSITY; HUMAN; INTRON; LINKAGE ANALYSIS; MALE; MICROSATELLITE MARKER; MUTATIONAL ANALYSIS; PEDIGREE ANALYSIS; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEQUENCE ANALYSIS; TOOTH MALFORMATION; CHINA; GENETIC LINKAGE; GENETICS; MUTATION; PEDIGREE;

ADULT; CHINA; DENTINOGENESIS IMPERFECTA; DNA PRIMERS; EXTRACELLULAR MATRIX PROTEINS; FEMALE; HUMANS; LINKAGE (GENETICS); MALE; MUTATION; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SEQUENCE ANALYSIS, DNA;

EID: 34848877727     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-8-52     Document Type: Article

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