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Showing results (101-110 of 105) with videos related to

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Brain : a Journal of Neurology|February 5, 2003
Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth diseaseA Jordanova, P De Jonghe, C F Boerkoel, et al.
Journal of Microscopy|January 28, 2015
Developing 3D SEM in a broad biological contextA Kremer, S Lippens, S Bartunkova, et al.
Neurology|July 15, 2011
Dominant GDAP1 mutations cause predominantly mild CMT phenotypesM Zimoń, J Baets, G M Fabrizi, et al.
Neurobiology of Disease|January 1, 1997
Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT ConsortiumH W Müller, U Suter, C Van Broeckhoven, et al.
Neurology|December 2, 2011
Distal myopathy with upper limb predominance caused by filamin C haploinsufficiencyV Guergueltcheva, K Peeters, J Baets, et al.
Pageof 11

Showing results (101-110 of 105) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 105 results.
Brain : a Journal of Neurology|February 5, 2003
Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth diseaseA Jordanova, P De Jonghe, C F Boerkoel, et al.
Journal of Microscopy|January 28, 2015
Developing 3D SEM in a broad biological contextA Kremer, S Lippens, S Bartunkova, et al.
Neurology|July 15, 2011
Dominant GDAP1 mutations cause predominantly mild CMT phenotypesM Zimoń, J Baets, G M Fabrizi, et al.
Neurobiology of Disease|January 1, 1997
Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT ConsortiumH W Müller, U Suter, C Van Broeckhoven, et al.
Neurology|December 2, 2011
Distal myopathy with upper limb predominance caused by filamin C haploinsufficiencyV Guergueltcheva, K Peeters, J Baets, et al.
Pageof 11