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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Uddin, Mohammed, Maksymowych, Walter P, Inman, Robert, Gladman, Dafna, Munn, Alexandra, Yazdani, Ramin, Pellett, Fawnda, Hamilton, Sean, O’Rielly, Darren D, Rahman, Proton
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2013
Témata:
Research Article
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky