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Parkinsonian features have been described in patients harboring variants in nuclear genes encoding for proteins involved in mitochondrial DNA maintenance, such as TWNK.

TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study

Valente, Enza Maria
;
2022-01-01

Abstract

Parkinsonian features have been described in patients harboring variants in nuclear genes encoding for proteins involved in mitochondrial DNA maintenance, such as TWNK.
2022
The Neurology category covers resources concerned with the central and peripheral nervous system including the brain, spinal cord, nerves, and fluids. Coverage includes general and clinical neurology including neurosurgery, neuropsychiatry, neuropsychology, neurophysiology, neuroradiology, neuropediatrics, neuropathology, and neurobiology. Resources on cerebrovascular diseases, movement and spinal disorders, pain, dementia, headache, aphasiology, brain injury, paraplegia, stroke, and acupuncture are also included.
MOVEMENT DISORDERS
sì
WOS:000821119700001
2-s2.0-85133456398
Esperti anonimi
Inglese
Internazionale
STAMPA
37
9
1938
1943
6
35792653
TWNK; Parkinson's disease; mitochondrial DNA; parkinsonism; twinkle; DNA, Mitochondrial; Humans; Mutation; Retrospective Studies; Mitochondrial Diseases; Parkinson Disease; Parkinsonian Disorders
sì
22
info:eu-repo/semantics/article
262
Percetti, Marco; Franco, Giulia; Monfrini, Edoardo; Caporali, Leonardo; Minardi, Raffaella; La Morgia, Chiara; Valentino, Maria Lucia; Liguori, Rocco;...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1465418
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