Supplemental material
Ophthalmic Genetics
Volume 40, 2019 - Issue 4
Case Reports
Homozygous sequestosome 1 (SQSTM1) mutation: a rare cause for childhood-onset progressive cerebellar ataxia with vertical gaze palsy
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Sruthi S NairDepartment of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Indiahttps://orcid.org/0000-0001-5463-5229
https://orcid.org/0000-0001-5463-5229, , & Reprints and Corporate Permissions
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