Mutations and mechanism: how PINK1 may contribute to risk of sporadic Parkinson's disease

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Mutations and mechanism: how PINK1 may contribute to risk of sporadic Parkinson's disease

Gandhi, S; Plun-Favreau, H; (2017) Mutations and mechanism: how PINK1 may contribute to risk of sporadic Parkinson's disease. Brain , 140 (1) pp. 2-5. 10.1093/brain/aww320. Green open access

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Abstract

This scientific commentary refers to ‘Heterozygous PINK1 p.G411S increases risk of Parkinson’s disease via a dominant-negative mechanism’, by Puschmann et al. (doi:10.1093/ brain/aww261).

Type:	Article
Title:	Mutations and mechanism: how PINK1 may contribute to risk of sporadic Parkinson's disease
Open access status:	An open access version is available from UCL Discovery
DOI:	10.1093/brain/aww320
Publisher version:	http://doi.org/10.1093/brain/aww320
Language:	English
Additional information:	This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords:	Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences, Neurosciences & Neurology, Mitophagy
UCL classification:	UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Clinical and Movement Neurosciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases
URI:	https://discovery.ucl.ac.uk/id/eprint/1544814

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