Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis

Human molecular genetics

Volumn 23, Issue 19, 2014, Pages 5271-5282

  Buchan, Jillian G ^a   Alvarado, David M ^b   Haller, Gabe E ^c   Cruchaga, Carlos ^a   Harms, Matthew B ^c   Zhang, Tianxiao ^b   Willing, Marcia C ^c   Grange, Dorothy K ^c   Braverman, Alan C ^a   Miller, Nancy H ^a   Morcuende, Jose A ^b   Tang, Nelson L eung Sang ^c   Lam, Tsz Ping ^b   Ng, Bobby K in Wah ^c   Cheng, Jack C hun Yiu ^c   Dobbs, Matthew B ^c   Gurnett, Christina A ^c  

^a UNIVERSITY OF IOWA   (United States)

^b Department of Orthopaedic Surgery Department of Neurology Department of Pediatrics ^*  (United States)

^c UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; FIBRILLIN; SMAD2 PROTEIN;

ADOLESCENT; ADULT; ALLELE; AMINO ACID SUBSTITUTION; ANCESTRY GROUP; CASE CONTROL STUDY; CHILD; FEMALE; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENETICS; HUMAN; MALE; MARFAN SYNDROME; METABOLISM; ODDS RATIO; PARASPINAL MUSCLE; PHOSPHORYLATION; SCOLIOSIS; SEVERITY OF ILLNESS INDEX; YOUNG ADULT;

ADOLESCENT; ADULT; ALLELES; AMINO ACID SUBSTITUTION; CASE-CONTROL STUDIES; CHILD; CONTINENTAL POPULATION GROUPS; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HUMANS; MALE; MARFAN SYNDROME; MICROFILAMENT PROTEINS; ODDS RATIO; PARASPINAL MUSCLES; PHOSPHORYLATION; SCOLIOSIS; SEVERITY OF ILLNESS INDEX; SMAD2 PROTEIN; YOUNG ADULT;

EID: 84964315986     PISSN: None     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu224     Document Type: Article

References (0)