For citations:

Shchagina O.A., Milovidova T.B., Bulah M.V., Polyakov A.V. The study of autosomal recessive CMT-disease with using a new medical technologies «One tube detection system for most common recessive CMT-mutation». Medical Genetics. 2016;15(3):35-39. (In Russ.) https://doi.org/10.1234/XXXX-XXXX-2016-3-35-39