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New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32

DOI

45

Citations

33

References

2013

Year

Carmen Serrano, Marc Corral‐Juan, Giovanni Stévanin, Héctor San Nicolás, Carles Roig, Jordi Corral, Berta Campos, Laura Jorge, Carlos Morcillo-Suárez, Arcadi Navarro,
JAMA Neurology

Abstract

We report a new subtype of SCA presenting in patients as slow progressing ataxia with altered vertical eye movements linked to a 11-megabase interval on 1p32. The Human Genome Nomenclature Committee has assigned this subtype of ataxia the designation SCA37.

References

YearCitations

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