A patient with Beta-Propeller Protein-Associated Neurodegeneration: a new missense mutation of the WDR45 gene
Authors
Anastasia Ivanova
Department of Cytoplasmic Hereditary, Institute of Genetics and Cytology of the National Academy of Sciences of Belarus, Minsk, Belarus
Sviatlana Kulikova
Neurological Department, Republican Research and Clinical Center of Neurology and Neurosurgery, Minsk, Belarus
Larysa Sivitskaya
Diagnostic Department, Genomed Health Care Centre, Warsaw, Poland
Nina Danilenko
Department of Cytoplasmic Hereditary, Institute of Genetics and Cytology of the National Academy of Sciences of Belarus, Minsk, Belarus
Oleg Davydenko
Department of Cytoplasmic Hereditary, Institute of Genetics and Cytology of the National Academy of Sciences of Belarus, Minsk, Belarus
Language: English
Submitted on: May 17, 2022
Accepted on: Jun 15, 2022
Published on: Jul 1, 2022
Published by: The Foundation of Epileptology
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2022 Anastasia Ivanova, Sviatlana Kulikova, Larysa Sivitskaya, Nina Danilenko, Oleg Davydenko, published by The Foundation of Epileptology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.