Associated Papers
Clinical analysis of Gabriele-de Vries caused by YY1 mutations and literature review.
Yang J et al.
Molecular Genetics & Genomic Medicine, 2024
YY1: A New Gene for Childhood Onset Dystonia with Prominent Oromandibular-Laryngeal Involvement?
Ferng A et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2022
Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations.
Macías-García D et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2022
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