DOI: 10.24075/brsmu.2019.034

ORIGINAL RESEARCH

Clinical and molecular-genetic profiles of patients with morphological indications of congenital multicore myopathy

Kozina AA1,5, Shatalov PA3,5, Baranich TI1, Artemieva SB3, Kupriyanova AG3, Baryshnikova NV1,5, Krasnenko AYu1,5, Ilinsky VV1,2,5, Sukhorukov VS1,4
About authors

1 Pirogov Russian National Research Medical University, Moscow, Russia

2 Institute of Biomedical Chemistry, Moscow, Russia

3 Veltischev Research and Clinical Institute for Pediatrics, Pirogov Russian National Research Medical University, Moscow, Russia

4 Research Center of Neurology, Moscow, Russia

5 Genotek Ltd., Moscow, Russia

Correspondence should be addressed: Anastasia A. Kozina
Nastavnichesky per 17, bld. 1, Moscow, 105120; ur.ketoneg@rotcod

About paper

Author contribution: Kozina AA — literature analysis, analysis and interpretation of exome sequencing data, manuscript preparation; Shatalov PA — data acquisition, microscopy, manuscript preparation; Baranich TI — microscopy; Artemieva SB — medical histories and neurological examinations; Kupriyanova AG — clinical data acquisition; Baryshnikova NV — literature analysis, analysis and interpretation of exome sequencing data, manuscript preparation; Krasnenko AYu — exome sequencing; Ilinsky VV — exome sequencing; Sukhorukov VS — study design, data acquisition.

Received: 2019-02-07 Accepted: 2019-04-19 Published online: 2019-04-30
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