Title: Adult cases of mitochondrial DNA depletion due to TK2 defect: an expanding spectrum
Authors: Béhin, A ×
Jardel, C
Claeys, Kristl
Fagart, J
Louha, M
Romero, N B
Laforêt, P
Eymard, B
Lombès, A #
Issue Date: Feb-2012
Publisher: Advanstar Communications
Series Title: Neurology vol:78 issue:9 pages:644-648
Article number: 10.1212/WNL.0b013e318248df2b
Abstract: In this study we aim to demonstrate the occurrence of adult forms of TK2 mutations causing progressive mitochondrial myopathy with significant muscle mitochondrial DNA (mtDNA) depletion.
ISSN: 0028-3878
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory for Muscle Diseases and Neuropathies
× corresponding author
# (joint) last author

Files in This Item:
File Description Status SizeFormat
Behin et al Neurology 2012.pdf Published 311KbAdobe PDFView/Open Request a copy

These files are only available to some KU Leuven Association staff members


All items in Lirias are protected by copyright, with all rights reserved.

© Web of science