WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta

New England Journal of Medicine

Volumn 368, Issue 19, 2013, Pages 1809-1816

  Laine, Christine M ^a,g   Joeng, Kyu Sang ^h   Campeau, Philippe M ^h   Kiviranta, Riku ^d,e   Tarkkonen, Kati ^d   Grover, Monica ^h   Lu, James T ^h   Pekkinen, Minna ^a   Wessman, Maija ^a,b   Heino, Terhi J ^d   Nieminen Pihala, Vappu ^d   Aronen, Mira ^a   Laine, Tero ^g   Kröger, Heikki ^f   Cole, William G ^j   Lehesjoki, Anna Elina ^a   Nevarez, Lisette ^k   Krakow, Deborah ^k,l   Curry, Cynthia J R ^m,n   Cohn, Daniel H ^k   Gibbs, Richard A ^h   Lee, Brendan H ^h,i   Mäkitie, Outi ^a,c   more..

^a UNIVERSITY OF HELSINKI   (Finland)

^b UNIVERSITY OF HELSINKI   (Finland)

^c UNIVERSITY OF HELSINKI AND HELSINKI UNIVERSITY HOSPITAL   (Finland)

^d UNIVERSITY OF TURKU   (Finland)

^e TURKU UNIVERSITY HOSPITAL   (Finland)

^f KUOPIO UNIVERSITY HOSPITAL   (Finland)

^g SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

^h BAYLOR COLLEGE OF MEDICINE   (United States)

ⁱ HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^j UNIVERSITY OF ALBERTA   (Canada)

^k UNIVERSITY OF CALIFORNIA   (United States)

^l UNIVERSITY OF CALIFORNIA   (United States)

^m UNIVERSITY OF CALIFORNIA   (United States)

ⁿ Genetic Medicine Central California   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE; GLYCINE; GUANINE; SERINE; THYMINE; WNT1 PROTEIN;

ADOLESCENT; ADULT; AGED; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BONE MARROW; BONE MINERALIZATION; CELL COMMUNICATION; CELL LINEAGE; CELL SUBPOPULATION; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DOMINANT INHERITANCE; FAMILY STUDY; FEMALE; GENE EXPRESSION; GENE TARGETING; GENETIC ASSOCIATION; HEMATOPOIETIC CELL; HEMATOPOIETIC STEM CELL; HETEROZYGOSITY; HUMAN; HUMAN CELL; IN VITRO STUDY; MALE; MISSENSE MUTATION; NONHUMAN; NUCLEIC ACID BASE SUBSTITUTION; ONSET AGE; OSTEOBLAST; OSTEOCYTE; OSTEOGENESIS IMPERFECTA; OSTEOPOROSIS; PRIORITY JOURNAL; PROTEIN DEFECT; RECESSIVE INHERITANCE; SCHOOL CHILD; SIBLING; SIGNAL TRANSDUCTION; WNT1 GENE;

EID: 84877595835     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMoa1215458     Document Type: Article

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