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

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dc.contributor.authorMišković, Nataša Dragašević (56418069100)
dc.contributor.authorDomingo, Aloysius (55577674500)
dc.contributor.authorDobričić, Valerija (22952783800)
dc.contributor.authorMax, Christoph (57188853526)
dc.contributor.authorBrænne, Ingrid (18233463200)
dc.contributor.authorPetrović, Igor (7004083314)
dc.contributor.authorGrütz, Karen (57120134300)
dc.contributor.authorPawlack, Heike (23490130300)
dc.contributor.authorTournev, Ivailo (6604049147)
dc.contributor.authorKalaydjieva, Luba (7006320678)
dc.contributor.authorSvetel, Marina (6701477867)
dc.contributor.authorLohmann, Katja (24067483500)
dc.contributor.authorKostić, Vladimir S (57189017751)
dc.contributor.authorWestenberger, Ana (55577873900)
dc.date.accessioned2025-07-02T12:21:39Z
dc.date.available2025-07-02T12:21:39Z
dc.date.issued2016
dc.description.abstract[No abstract available]
dc.identifier.urihttps://doi.org/10.1002/mds.26816
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84999633551&doi=10.1002%2fmds.26816&partnerID=40&md5=c30b09f9b9487ccda687b8f0e6570068
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/13269
dc.subjectANO10
dc.subjectautosomal recessive cerebellar ataxia
dc.subjectfounder mutation
dc.subjectgenotype-phenotype correlation
dc.subjectwhole-exome sequencing
dc.titleSeemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia
dspace.entity.typePublication

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