In Japanese, Koreans and Caucasians, narcolepsy/hypocretin deficiency is tightly associated with the DRB1*15:01-DQA1*01:02-DQB1*06:02 haplotype. Studies in African-Americans suggest a primary effect of DQB1*06:02, but this observation has been difficult to confirm in other populations because of high linkage disequilibrium between DRB1*15:01/3 and DQB1*06:02 in most populations. In this study, we studied human leucocyte antigen (HLA) class II in 202 Chinese narcolepsy patients (11% from South China) and found all patients to be DQB1*06:02 positive. Comparing cases with 103 unselected controls, and 110 and 79 controls selected for the presence of DQB1*06:02 and DRB1*15:01, we found that the presence of DQB1*06:02 and not DRB1*15:01 was assoc...
Narcolepsy is a unique model for dysfunction in mechanisms that regulate sleep and wakefulness. the ...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...
Human narcolepsy-cataplexy, a sleep disorder associated with a centrally mediated hypocretin (orexin...
The purpose of this study was to investigate the association of human leukocyte antigen (HLA) class ...
[[abstract]]Background: Narcolepsy is a rare, chronic, disabling neuropsychiatric disorder character...
Human narcolepsy-cataplexy, a sleep disorder associated with a centrally mediated hypocretin (orexin...
Type 1 narcolepsy, a disorder caused by a lack of hypocretin (orexin), is so strongly associated wit...
Type 1 narcolepsy, a disorder caused by a lack of hypocretin (orexin), is so strongly associated wit...
International audienceType 1 narcolepsy, a disorder caused by a lack of hypocretin (orexin), is so s...
A systematic haplotype and sequencing analysis of the HLA -DR and - DQ region in patients with narc...
none34siType 1 narcolepsy, a disorder caused by a lack of hypocretin (orexin), is so strongly associ...
To identify rare allelic variants and HLA alleles in narcolepsy patients with hypocretin (orexin, HC...
Narcolepsy is a rare sleep disorder with the strongest human leukocyte antigen (HLA) association eve...
To identify rare allelic variants and HLA alleles in narcolepsy patients with hypocretin (orexin, HC...
Narcolepsy is a unique model for dysfunction in mechanisms that regulate sleep and wakefulness. the ...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...
Human narcolepsy-cataplexy, a sleep disorder associated with a centrally mediated hypocretin (orexin...
The purpose of this study was to investigate the association of human leukocyte antigen (HLA) class ...
[[abstract]]Background: Narcolepsy is a rare, chronic, disabling neuropsychiatric disorder character...
Human narcolepsy-cataplexy, a sleep disorder associated with a centrally mediated hypocretin (orexin...
Type 1 narcolepsy, a disorder caused by a lack of hypocretin (orexin), is so strongly associated wit...
Type 1 narcolepsy, a disorder caused by a lack of hypocretin (orexin), is so strongly associated wit...
International audienceType 1 narcolepsy, a disorder caused by a lack of hypocretin (orexin), is so s...
A systematic haplotype and sequencing analysis of the HLA -DR and - DQ region in patients with narc...
none34siType 1 narcolepsy, a disorder caused by a lack of hypocretin (orexin), is so strongly associ...
To identify rare allelic variants and HLA alleles in narcolepsy patients with hypocretin (orexin, HC...
Narcolepsy is a rare sleep disorder with the strongest human leukocyte antigen (HLA) association eve...
To identify rare allelic variants and HLA alleles in narcolepsy patients with hypocretin (orexin, HC...
Narcolepsy is a unique model for dysfunction in mechanisms that regulate sleep and wakefulness. the ...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...