Author: Zeldenrust Steven R.
Publisher: Informa Healthcare
ISSN: 1350-6129
Source: Amyloid: The Journal of Protein Folding Disorders, Vol.19, Iss.1, 2012-06, pp. : 22-24
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Related content
Early- and late-onset inherited erythromelalgia: genotype–phenotype correlation
Brain, Vol. 132, Iss. 7, 2009-07 ,pp. :
MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2
By Verhoeven Kristien Claeys Kristl G. Schröder J. Michael Weis Joachim Ceuterick Chantal Jordanova Albena Nelis Eva De Vriendt Els Van Hul Matthias Seeman Pavel Mazanec Radim Saifi Gulam Mustafa Szigeti Kinga Mancias Pedro Butler Ian J. Kochanski Andrzej Ryniewicz Barbara De Bleecker Jan Van den Bergh Peter Verellen Christine Van Coster Rudy Goemans Nathalie Auer-Grumbach Michaela Robberecht Wim Milic Rasic Vedrana Nevo Yoram Tournev Ivajlo Guergueltcheva Velina Roelens Filip Vieregge Peter Vinci Paolo Moreno Maria Teresa Christen H.-J. Shy Michael E. Lupski James R. Vance Jeffery M. De Jonghe Peter Timmerman Vincent
Brain, Vol. 129, Iss. 8, 2006-08 ,pp. :