UGT2B17 copy number gain in a large ankylosing spondylitis multiplex family

BACKGROUND: The primary objective of this study is to identify novel copy number variations (CNVs) associated with familial ankylosing spondylitis (AS). A customized genome-wide microarray was designed to detect CNVs and applied to a multiplex AS family with six (6) affected family members. CNVs wer...

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Detalles Bibliográficos
Autores principales: Uddin, Mohammed, Maksymowych, Walter P, Inman, Robert, Gladman, Dafna, Munn, Alexandra, Yazdani, Ramin, Pellett, Fawnda, Hamilton, Sean, O’Rielly, Darren D, Rahman, Proton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751806/
https://www.ncbi.nlm.nih.gov/pubmed/23927372
http://dx.doi.org/10.1186/1471-2156-14-67

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751806/
https://www.ncbi.nlm.nih.gov/pubmed/23927372
http://dx.doi.org/10.1186/1471-2156-14-67

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