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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Bibliographic Details
Main Authors:	Uddin, Mohammed, Maksymowych, Walter P, Inman, Robert, Gladman, Dafna, Munn, Alexandra, Yazdani, Ramin, Pellett, Fawnda, Hamilton, Sean, O’Rielly, Darren D, Rahman, Proton
Format:	Artigo
Language:	Inglês
Published:	BioMed Central 2013
Subjects:	Research Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC3751806/ https://ncbi.nlm.nih.gov/pubmed/23927372 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-14-67
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UGT2B17 copy number gain in a large ankylosing spondylitis multiplex family

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