Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.
The major histocompatibility complex (MHC) is recognised as one of the most important genetic regions in relation to common human disease. Advancement in identification of MHC genes that confer susceptibility to disease requires greater knowledge of sequence variation across the complex. Highly dupl...
Format: | Article |
---|---|
Language: | English |
Published: |
Public Library of Science (PLoS)
2006-01-01
|
Series: | PLoS Genetics |
Online Access: | http://dx.doi.org/10.1371/journal.pgen.0020009 |
Similar Items
-
Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.
by: James A Traherne, et al.
Published: (2006-01-01) -
Haplotype-specific linkage disequilibrium patterns define the genetic topography of the human MHC.
by: Ahmad, T, et al.
Published: (2003) -
Unique Allelic eQTL Clusters in Human MHC Haplotypes
by: Tze Hau Lam, et al.
Published: (2017-08-01) -
PCR-RFLP Genotyping of Murine MHC Haplotypes
by: Stanford L. Peng, et al.
Published: (1996-09-01) -
LTA-TNF HAPLOTYPE STUDIES IDENTIFY ADDITIONAL RHEUMATOID ARTHRITIS SUSCEPTIBILITY REGIONS IN THE MHC
by: Newton, J, et al.
Published: (2002)