A novel homozygous SQSTM1 frameshift variant in a Filipino adolescent with childhood-onset ataxia and gaze palsy

Parkinsonism & Related Disorders 2026

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Authors: Lowrence Precious Dichoso, Gerard Saranza, Chin-Hsien Lin
DOI: 10.1016/j.parkreldis.2026.108233
Cited by: 2
References: 18

Fields of Study & Subjects

Genetic Neurodegenerative Diseases Hereditary Neurological Disorders Glycogen Storage Diseases and Myoclonus

Publication details

Journal / source
Parkinsonism & Related Disorders
Publisher
Elsevier BV
Pages
108233–108233
Publication date
1 February 2026
Language
EN