Altmetric

Novel deletions in TPM3 define a hypercontractile phenotype with marked congenital muscle stiffness: Expanding the spectrum of TPM3 related disease

File Description SizeFormat 
ana accepted paper.pdfAccepted version308.55 kBAdobe PDFView/Open
Title: Novel deletions in TPM3 define a hypercontractile phenotype with marked congenital muscle stiffness: Expanding the spectrum of TPM3 related disease
Authors: Donkervoort, S
Neu, M
Kirschner, J
Yang, ML
Marston, SB
Gibbons, MA
Hu, Y
de Winter, JM
Ottenheijm, CAC
Rutkowski, A
Krueger, M
McNamara, E
Ong, R
Nowak, K
Clarke, NF
Boennemann, CG
Item Type: Conference Paper
Issue Date: 2-Sep-2014
Date of Acceptance: 2-Sep-2014
URI: http://hdl.handle.net/10044/1/26634
DOI: https://dx.doi.org/10.1016/j.nmd.2014.06.348
ISSN: 1873-2364
Publisher: Elsevier
Start Page: 898
End Page: 899
Journal / Book Title: Neuromuscular Disorders
Volume: 24
Issue: 9-10
Copyright Statement: © 2014, Elsevier. Licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/
Conference Name: 19th International Congress of the World Muscle-Society
Keywords: Science & Technology
Life Sciences & Biomedicine
Clinical Neurology
Neurosciences
Neurosciences & Neurology
Publication Status: Published
Start Date: 2014-10-07
Finish Date: 2014-10-11
Conference Place: Berlin, Germany
Appears in Collections:National Heart and Lung Institute
Faculty of Medicine



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Creative Commonsx