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

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Date

2016

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Research Projects

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[No abstract available]

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ANO10, autosomal recessive cerebellar ataxia, founder mutation, genotype-phenotype correlation, whole-exome sequencing

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https://doi.org/10.1002/mds.26816
 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84999633551&doi=10.1002%2fmds.26816&partnerID=40&md5=c30b09f9b9487ccda687b8f0e6570068
 https://remedy.med.bg.ac.rs/handle/123456789/13269

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Publikacije / Publications