Familial tremor linked to a heterozygous variant in the Ceruloplasmin gene.

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Bibliographic Details
Title: Familial tremor linked to a heterozygous variant in the Ceruloplasmin gene.
Authors: De Vita G; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy; CEINGE Advanced Biotechnology, Naples, Italy., Blasio G; CEINGE Advanced Biotechnology, Naples, Italy., Riccio G; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy., Coppola R; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy., Dell'Aversana D; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy., Coppola A; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy., Cocozza S; Departments of Advanced Biomedical Sciences and Electrical Engineering and Information Technology, University of Naples Federico II, Naples, Italy., Gragnano E; Departments of Advanced Biomedical Sciences and Electrical Engineering and Information Technology, University of Naples Federico II, Naples, Italy., Esposito M; Clinical Neurophysiology Unit, Cardarelli Hospital, Naples, Italy., De Michele G; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy., De Rosa A; Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy. Electronic address: anna.derosa1@unina.it.
Source: Parkinsonism & related disorders [Parkinsonism Relat Disord] 2026 Jun; Vol. 147, pp. 108333. Date of Electronic Publication: 2026 Apr 27.
Publication Type: Letter
Journal Info: Publisher: Elsevier Science Country of Publication: England NLM ID: 9513583 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-5126 (Electronic) Linking ISSN: 13538020 NLM ISO Abbreviation: Parkinsonism Relat Disord Subsets: MEDLINE; In Process
Database: MEDLINE Ultimate
Description
ISSN:1873-5126
DOI:10.1016/j.parkreldis.2026.108333