A novel nonsense mutation in PAX9 is associated with sporadic hypodontia

Mutagenesis

Volumn 27, Issue 3, 2012, Pages 313-317

  Zhu, Junxia ^a   Yang, Xiang ^a   Zhang, Chenying ^a   Ge, Lihong ^a   Zheng, Shuguo ^a  

^a PEKING UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; TRANSCRIPTION FACTOR MSX1; TRANSCRIPTION FACTOR PAX9;

ARTICLE; CASE REPORT; CHILD; CHINESE; DECIDUOUS TOOTH; EXON; FEMALE; GENE FREQUENCY; GENE SEQUENCE; HAPLOINSUFFICIENCY; HETEROZYGOSITY; HUMAN; HYPODONTIA; LYMPHOCYTE; MALE; NONSENSE MUTATION; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DEGRADATION; PROTEIN LOCALIZATION; STOP CODON;

ANIMALS; ANODONTIA; BASE SEQUENCE; CERCOPITHECUS AETHIOPS; CODON, NONSENSE; COS CELLS; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, REPORTER; GENETIC ASSOCIATION STUDIES; HAPLOINSUFFICIENCY; HEK293 CELLS; HUMANS; LUCIFERASES, RENILLA; MALE; MSX1 TRANSCRIPTION FACTOR; PAX9 TRANSCRIPTION FACTOR; PEDIGREE; PROTEIN TRANSPORT; TRANSCRIPTION, GENETIC;

EID: 84860118147     PISSN: 02678357     EISSN: 14643804     Source Type: Journal    
DOI: 10.1093/mutage/ger080     Document Type: Article

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