Publications by authors named "Ludmila Bessonova"

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Rare Cause 5q SMA: Molecular Genetic and Clinical Analyses of Intragenic Subtle Variants in the SMN Locus.
Kristina Mikhalchuk, Viktoria Zabnenkova, Svetlana Braslavskaya, Alena Chukhrova, Nina Ryadninskaya, Ludmila Bessonova

Clin Genet· July 2025

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Common Variants in the Gene with Unclear Pathogenicity as the Cause of Oculocutaneous Albinism in a Cohort of Russian Patients.
Olga Shchagina, Anna Stepanova, Polina Mishakova, Vitaliy Kadyshev, Nina Demina, Ludmila Bessonova

Biomedicines· October 2024

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Complex Diagnostics of Non-Specific Intellectual Developmental Disorder.
Olga Levchenko, Elena Dadali, Ludmila Bessonova, Nina Demina, Galina Rudenskaya

Int J Mol Sci· July 2022

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A Family Case of Congenital Myasthenic Syndrome-22 Induced by Different Combinations of Molecular Causes in Siblings.
Olga Shchagina, Ludmila Bessonova, Igor Bychkov, Tatiana Beskorovainaya, Aleksander Poliakov

Genes (Basel)· July 2020

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Novel KIAA1109 variants affecting splicing in a Russian family with ALKURAYA-KUČINSKAS syndrome.
Alexandra Filatova, Valeria Freire, Ekaterina Lozier, Fedor Konovalov, Ludmila Bessonova

Clin Genet· March 2019

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