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Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis.
Buchan, Jillian G; Alvarado, David M; Haller, Gabe E; Cruchaga, Carlos; Harms, Matthew B; Zhang, Tianxiao; Willing, Marcia C; Grange, Dorothy K; Braverman, Alan C; Miller, Nancy H; Morcuende, Jose A; Tang, Nelson Leung-Sang; Lam, Tsz-Ping; Ng, Bobby Kin-Wah; Cheng, Jack Chun-Yiu; Dobbs, Matthew B; Gurnett, Christina A.
Afiliação
  • Buchan JG; Department of Genetics.
  • Alvarado DM; Department of Orthopaedic Surgery.
  • Haller GE; Department of Orthopaedic Surgery.
  • Cruchaga C; Department of Psychiatry.
  • Harms MB; Department of Neurology.
  • Zhang T; Department of Psychiatry.
  • Willing MC; Department of Pediatrics.
  • Grange DK; Department of Pediatrics.
  • Braverman AC; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Miller NH; Department of Orthopaedic Surgery, University of Colorado, Denver, CO 80202, USA.
  • Morcuende JA; Department of Orthopaedic Surgery, University of Iowa, Iowa City, IA 52242, USA.
  • Tang NL; The Chinese University of Hong Kong, Hong Kong, China and.
  • Lam TP; The Chinese University of Hong Kong, Hong Kong, China and.
  • Ng BK; The Chinese University of Hong Kong, Hong Kong, China and.
  • Cheng JC; The Chinese University of Hong Kong, Hong Kong, China and.
  • Dobbs MB; Department of Orthopaedic Surgery St. Louis Shriners Hospital for Children, St. Louis, MO 63131, USA.
  • Gurnett CA; Department of Orthopaedic Surgery Department of Neurology Department of Pediatrics, gurnettc@neuro.wustl.edu.
Hum Mol Genet ; 23(19): 5271-82, 2014 Oct 01.
Article em En | MEDLINE | ID: mdl-24833718
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escoliose / Variação Genética / Proteínas dos Microfilamentos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Ano de publicação: 2014 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escoliose / Variação Genética / Proteínas dos Microfilamentos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Ano de publicação: 2014 Tipo de documento: Article