Cite
HARVARD Citation
Li, L. et al. (2022). Whole‐Exome Sequencing Identified Rare Variants in PCDHGB1 in Patients with Adult‐Onset Dystonia. Movement disorders. 37 (5), pp. 1099-1101. [Online].
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Li, L. et al. (2022). Whole‐Exome Sequencing Identified Rare Variants in PCDHGB1 in Patients with Adult‐Onset Dystonia. Movement disorders. 37 (5), pp. 1099-1101. [Online].