|?|| (C;C) (C;G) (G;G) ||28|
] HLA polymorphisms in Italian children with autism spectrum disorders: Results of a family based linkage study
[PMID 17509152] Variation of the myelin oligodendrocyte glycoprotein gene is not primarily associated with multiple sclerosis in the Sardinian population.
[PMID 17928868] A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy.
[PMID 19167444] Family-based transmission analysis of HLA genetic markers in Sardinian children with autistic spectrum disorders.
[PMID 20800907] Common variation in the MOG gene influences transcript splicing in humans.
[PMID 23032943] The association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected relatives
|| not reviewed
|| Insufficiently evaluated not reviewed