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Ophthalmic Genetics Volume 40, 2019 - Issue 4
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Case Reports

Homozygous sequestosome 1 (SQSTM1) mutation: a rare cause for childhood-onset progressive cerebellar ataxia with vertical gaze palsy

Veena VedarthamDepartment of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India
,
Soumya SundaramDepartment of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, IndiaCorrespondence[email protected] [email protected]
,
Sruthi S NairDepartment of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, IndiaORCID Iconhttps://orcid.org/0000-0001-5463-5229
ORCID Icon,
Aparna GanapathyDepartment of Clinical Genomics, Strand Center for Genomics and Personalized Medicine, Bangalore, India
,
Ashraf MannanDepartment of Clinical Genomics, Strand Center for Genomics and Personalized Medicine, Bangalore, India
&
Ramshekhar MenonDepartment of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India
Pages 376-379 | Received 30 Jun 2019, Accepted 02 Sep 2019, Published online: 16 Sep 2019

References

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