Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia

Mišković, Nataša Dragašević (56418069100)Nataša Dragašević (56418069100)MiškovićDomingo, Aloysius (55577674500)Aloysius (55577674500)DomingoDobričić, Valerija (22952783800)Valerija (22952783800)DobričićMax, Christoph (57188853526)Christoph (57188853526)MaxBrænne, Ingrid (18233463200)Ingrid (18233463200)BrænnePetrović, Igor (7004083314)Igor (7004083314)PetrovićGrütz, Karen (57120134300)Karen (57120134300)GrützPawlack, Heike (23490130300)Heike (23490130300)PawlackTournev, Ivailo (6604049147)Ivailo (6604049147)TournevKalaydjieva, Luba (7006320678)Luba (7006320678)KalaydjievaSvetel, Marina (6701477867)Marina (6701477867)SvetelLohmann, Katja (24067483500)Katja (24067483500)LohmannKostić, Vladimir S (57189017751)Vladimir S (57189017751)KostićWestenberger, Ana (55577873900)Ana (55577873900)Westenberger2025-07-022025-07-022016https://doi.org/10.1002/mds.26816https://www.scopus.com/inward/record.uri?eid=2-s2.0-84999633551&doi=10.1002%2fmds.26816&partnerID=40&md5=c30b09f9b9487ccda687b8f0e6570068https://remedy.med.bg.ac.rs/handle/123456789/13269[No abstract available]ANO10autosomal recessive cerebellar ataxiafounder mutationgenotype-phenotype correlationwhole-exome sequencingSeemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia