Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Connexin32 in hereditary neuropathies

D H Neuberg1, U Suter

  • 1Department of Biology, Swiss Federal Institute of Technology, ETH Hönggerberg, Zürich, Switzerland.

Advances in Experimental Medicine and Biology
|January 15, 2000
PubMed
Summary

No abstract available in PubMed .

Related Experiment Videos

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Dominant GDAP1 mutations cause predominantly mild CMT phenotypes.

Neurology·2011
Same author

Phosphoinositides and Charcot-Marie-tooth disease: new keys to old questions.

Cellular and molecular life sciences : CMLS·2007
Same author

118th ENMC International Workshop on Advances in Myotubular Myopathy. 26-28 September 2003, Naarden, The Netherlands. (5th Workshop of the International Consortium on Myotubular Myopathy).

Neuromuscular disorders : NMD·2004
Same author

The causes of Charcot-Marie-Tooth disease.

Cellular and molecular life sciences : CMLS·2003
Same author

Steroid hormones and neurosteroids in normal and pathological aging of the nervous system.

Progress in neurobiology·2003
Same author

Differential cyclin D1 requirements of proliferating Schwann cells during development and after injury.

Molecular and cellular neurosciences·2001