Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis

• Asıl Yazarlar: Salvi Fabrizio (Yazar), Yuryev Anton (Yazar), Balboni Alessandra (Yazar), Gualandi Francesca (Yazar), Neri Marcella (Yazar), Bovolenta Matteo (Yazar), Ferlini Alessandra (Yazar), Gemmati Donato (Yazar), Liboni Alberto (Yazar), Zamboni Paolo (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: BMC, 2010-04-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Multiple sclerosis (MS) is a complex disorder thought to result from an interaction between environmental and genetic predisposing factors which have not yet been characterised, although it is known to be associated with the HLA regi...