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

Mov Disord. 2016 Dec;31(12):1929-1931. doi: 10.1002/mds.26816. Epub 2016 Oct 27.

¹ Clinic of Neurology, Faculty of Medicine, Clinical Centre of Serbia, University of Belgrade, Belgrade, Serbia.
² Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
³ Graduate School for Computing in Medicine and Life Science, University of Lübeck, Lübeck, Germany.
⁴ Institute for Integrative and Experimental Genomics, University of Lübeck, Lübeck, Germany.
⁵ Clinic of Nervous Diseases, University Hospital Aleksandrovska, Department of Neurology, Sofia Medical University, Sofia.
⁶ Department of Cognitive Science and Psychology, New Bulgarian University, Sofia.
⁷ Harry Perkins Institute of Medical Research and Centre for Medical Research, The University of Western Australia, Perth, Australia.

No abstract available

Keywords: ANO10; autosomal recessive cerebellar ataxia; founder mutation; genotype-phenotype correlation; whole-exome sequencing.

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