Sequestosome 1: Mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone

Journal of Bone and Mineral Research

Volumn 22, Issue SUPPL. 2, 2007, Pages

  Morissette, Jean ^a   Laurin, Nancy ^b   Brown, Jacques P ^a  

^a LAVAL UNIVERSITY   (Canada)

^b UNIVERSITY HEALTH NETWORK   (Canada)

Author keywords

Genetics; Paget's disease of bone; Penetrance; Phenotype; Sequestosome1 p62

Indexed keywords

ADULT; AGED; ARTICLE; CANADA; FAMILIAL DISEASE; GENE; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; GENETIC SCREENING; HAPLOTYPE; HUMAN; MUTATION RATE; PAGET BONE DISEASE; PENETRANCE; PHENOTYPE; SEQUESTOSOME 1; GENETICS; HETEROZYGOTE DETECTION; MUTATION; NUCLEOTIDE SEQUENCE;

PRIMER DNA; SIGNAL TRANSDUCING ADAPTOR PROTEIN; SQSTM1 PROTEIN, HUMAN; UNCLASSIFIED DRUG;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; BASE SEQUENCE; DNA PRIMERS; GENETIC SCREENING; HAPLOTYPES; HETEROZYGOTE DETECTION; HUMANS; MUTATION; OSTEITIS DEFORMANS; PHENOTYPE;

EID: 34247861003     PISSN: 08840431     EISSN: None     Source Type: Journal    
DOI: 10.1359/JBMR.06S207     Document Type: Article

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