Olga A. Levchenko

Moscow, MOW 115522, Russian Federation

Last Updated: 09/26/2026

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Found 13 publications

The Promise and Pitfalls of AAV-Mediated Gene Therapy for Duchenne Muscular Dystrophy.

The Promise and Pitfalls of AAV-Mediated Gene Therapy for Duchenne Muscular Dystrophy.

Journal: Current issues in molecular biology

Published: December 01, 2025

Generation of an Induced Pluripotent Stem Cell Line from a Duchenne Muscular Dystrophy Patient Carrying the DMD p.Ser429Ter (c.1286C>G) Nonsense Mutation.

Generation of an Induced Pluripotent Stem Cell Line from a Duchenne Muscular Dystrophy Patient Carrying the DMD p.Ser429Ter (c.1286C>G) Nonsense Mutation.

Journal: Bulletin of experimental biology and medicine

Published: September 04, 2025

Clinical and molecular genetic features of cases of Floating-Harbor syndrome

Clinical and molecular genetic features of cases of Floating-Harbor syndrome

Journal: Problemy endokrinologii

Published: October 24, 2024

Clinical Case of Mild Tatton-Brown-Rahman Syndrome Caused by a Nonsense Variant in DNMT3A Gene.

Clinical Case of Mild Tatton-Brown-Rahman Syndrome Caused by a Nonsense Variant in DNMT3A Gene.

Journal: Clinics and practice

Published: December 11, 2023

Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders.

Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 07, 2023

Unexpected extra exon skipping in the DYSF gene during restoring the reading frame by CRISPR/Cas9.

Unexpected extra exon skipping in the DYSF gene during restoring the reading frame by CRISPR/Cas9.

Journal: Bio Systems

Published: August 15, 2023

The Missing Piece of the Puzzle: Unveiling the Role of PTPN11 Gene in Multiple Osteochondromas in a Large Cohort Study.

The Missing Piece of the Puzzle: Unveiling the Role of PTPN11 Gene in Multiple Osteochondromas in a Large Cohort Study.

Journal: Human mutation

Published: June 09, 2023

Homozygous deep intronic variant in SNX14 cause autosomal recessive Spinocerebellar ataxia 20: a case report.

Homozygous deep intronic variant in SNX14 cause autosomal recessive Spinocerebellar ataxia 20: a case report.

Journal: Frontiers in genetics

Published: April 11, 2023

Complex Diagnostics of Non-Specific Intellectual Developmental Disorder.

Complex Diagnostics of Non-Specific Intellectual Developmental Disorder.

Journal: International journal of molecular sciences

Published: May 20, 2022

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 19, 2020

Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy.

Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy.

Journal: American journal of human genetics

Published: July 02, 2019

Massive parallel sequencing for molecular-genetic diagnosis of mental retardation

Massive parallel sequencing for molecular-genetic diagnosis of mental retardation

Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

Published: January 31, 2019

Showing 1-12 of 13

Last Updated: 09/26/2026