A patient with Beta-Propeller Protein-Associated Neurodegeneration: a new missense mutation of the WDR45 gene Cover

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A patient with Beta-Propeller Protein-Associated Neurodegeneration: a new missense mutation of the WDR45 gene

Journal of Epileptology

By: Anastasia Ivanova, Sviatlana Kulikova, Larysa Sivitskaya, Nina Danilenko and Oleg Davydenko

Open Access

|Jul 2022

Authors

Anastasia Ivanova

a.s.ivanova97@gmail.com

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

DOI: https://doi.org/10.2478/joepi-2022-0001 | Journal eISSN: 2299-9728 | Journal ISSN: 2300-0147

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Language: English

Submitted on: May 17, 2022

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Accepted on: Jun 15, 2022

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Published on: Jul 1, 2022

Published by: The Foundation of Epileptology

In partnership with: Paradigm Publishing Services

Publication frequency: 2 issues per year

Keywords:

developmental delay

Related subjects:

Clinical medicine,

Clinical medicine, other,

Pharmacology, toxicology,

Clinical pharmacy

© 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.