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VPS13D: One Family, Same Mutations, Two Phenotypes.
Petry-Schmelzer JN, Keller N, Karakaya M, Wirth B, Fink GR, Wunderlich G. Petry-Schmelzer JN, et al. Among authors: keller n. Mov Disord Clin Pract. 2021 May 5;8(5):803-806. doi: 10.1002/mdc3.13232. eCollection 2021 Jul. Mov Disord Clin Pract. 2021. PMID: 34307758 Free PMC article. No abstract available.
954 results