http://www.neurology.org/cgi/content/abstract/58/4/658
Neurology 2002;58:658-660
A. N. Boiko, MD;, E. I. Gusev, MD;,
M. A. Sudomoina, PhD;, A. D. Alekseenkov, MSc;, O. G. Kulakova, PhD;, O.
V. Bikova, MD;, O. I. Maslova, MD;, M. R. Guseva, MD;, S. Y. Boiko, MD;,
M. E. Guseva, MD; and O. O. Favorova, PhD
From the Department of Neurology
and Neurosurgery (Drs. A. Boiko, Gusev, M.R. Guseva, S. Boiko, and M.E.
Guseva) and the Department of Molecular Biology and Medical Biotechnology
(Drs. Sudomoina, Kulakova, Favorova, and Alekseenkov), Russian State Medical
University, Moscow; and the Psychoneurological Department (Drs. Bikova
and Maslova), Pediatric Institute of the Russian Academy of Medical Sciences,
Moscow, Russia.
The aim of this study was to determine the role of the HLA-DRB1 gene [6p21] in susceptibility to juvenile MS (JMS) (age at onset 15 years) of children of Russian descent.
Association of DR2(15) with JMS has been found by the comparison of patients with JMS with both unrelated and affected family-based healthy controls.
The linkage of DR2(15) with JMS was shown by transmission disequilibrium test.
There were no significant differences
in the frequencies of DRB1 alleles and genotypes between 56 patients with
JMS and 234 patients with MS with age at onset 16 years.
© 2002 American Academy of Neurology