Вариации числа копий последовательности ДНК гена TM2D3 при аутизме: идентификация гена-кандидата заболевания с помощью биоинформатического анализа результатов полногеномного сканирования
About the Authors
Наталья ШмитоваRussian Federation
Ю. Юров
Russian Federation
С. Ворсанова
Russian Federation
И. Юров
Russian Federation
References
1. Iourov I.Y., Vorsanova S.G., Kurinnaia O.S., Zelenova M.A., Silvanovich A.P., Yurov Y.B. Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies. Molecular Cytogenetics. 2012;5(1):46. http://dx.doi.org/10.1186/1755-8166-5-46
2. Vorsanova S.G., Voinova V.Yu., Yurov I.Y., Kurinnaya O.S., Demidova I.A., Yurov Y.B. Cytogenetic, molecular- cytogenetic, and clinical-genealogical studies of mothers of children with autism: a search of familial genetic markers of autistic disorders. Neuroscience and Behavioural Physiology. 2010;40(7):745-756. http://dx.doi.org/10.1007/s11055-010-9321-5
3. Yurov Y.B., Vorsanova S.G., Iourov I.Y. et al. Unexplained 75 autism is frequently associated with low-level mosaic aneuploidy. J. Med. Genet. 2007;44:521-525. http://dx.doi.org/10.1136/jmg.2007.049312
Review
For citations:
, , , . Psychiatry (Moscow) (Psikhiatriya). 2015;(4):74а-75. (In Russ.)