Editorial: Copy Number Variation in Rare Disorders

Front Genet. 2022 Apr 5:13:898059. doi: 10.3389/fgene.2022.898059. eCollection 2022.

Authors

Katalin Komlósi¹, Attila Gyenesei², Judit Bene³

Affiliations

¹ Institute of Human Genetics, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
² Bioinformatics Research Group, Genomics and Bioinformatics Core Facility, Szentagothai Research Center, University of Pécs, Pécs, Hungary.
³ Department of Medical Genetics, Clinical Centre, Medical School, University of Pécs, Pécs, Hungary.

No abstract available

Keywords: Mendelian disease; copy number variation (CNV); genomic disorders; genomic rearrangement; rare disorders.

Publication types

Editorial