Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees

Bone

Volumn 35, Issue 1, 2004, Pages 277-282

  Good, David A ^a,c   Busfield, Frances ^a   Fletcher, Barbara H ^a   Lovelock, Paul K ^a   Duffy, David L ^b   Kesting, Janine B ^a   Andersen, John ^a   Shaw, Joanne T E ^a  

^a PRINCESS ALEXANDRA HOSPITAL   (Australia)

^b QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

^c QUEENSLAND UNIVERSITY OF TECHNOLOGY   (Australia)

Author keywords

Genetics; Linkage analysis; Paget's disease of bone; Sequestosome 1

Indexed keywords

UBIQUITIN;

ADULT; AMINO ACID SEQUENCE; ARTICLE; AUSTRALIA; CARBOXY TERMINAL SEQUENCE; CHROMOSOME 5Q; CLINICAL ARTICLE; CONTROLLED STUDY; EXON; FAMILIAL DISEASE; GENE DELETION; GENE MUTATION; GENETIC CODE; GENETIC LINKAGE; HUMAN; PAGET BONE DISEASE; PEDIGREE; PREDICTION; PROTEIN BINDING; PROTEIN DOMAIN; SEQUENCE ANALYSIS; STOP CODON;

AMINO ACID SEQUENCE; AUSTRALIA; CHROMOSOMES, HUMAN, PAIR 5; EXONS; HUMANS; LOD SCORE; MOLECULAR SEQUENCE DATA; MUTATION; OSTEITIS DEFORMANS; PEDIGREE; PROTEINS;

EID: 2942709744     PISSN: 87563282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bone.2004.01.010     Document Type: Article

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