N.P.3 05 Mitofusin 2 mutations are a major cause for autosomal dominant axonal CMT neuropathy
K. Verhoeven, K.G. Claeys, S. Züchner, J.M. Schröder, J.M. Vance, V. Timmerman, P. De JongheVolume:
16
Year:
2006
Language:
english
DOI:
10.1016/j.nmd.2006.05.081
File:
PDF, 55 KB
english, 2006