The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound

Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

[search][options]

Editor

Personal info

View

About

Terms

Javascript disabled

Please enable Javascript support in your browser to use this application.

Instructions on how to enable JavaScript on different browsers can be found here: http://www.google.com/support/bin/answer.py?answer=23852.

Kinji Ohno

Department of Neurology and Neuromuscular Research Laboratory

Mayo Clinic

200 First Street SW

Rochester

USA

[email]@mayo.edu

Name/email consistency: high

[Claim this account]

Affiliations

Department of Neurology and Neuromuscular Research Laboratory, Mayo Clinic, 200 First Street SW, Rochester, USA. 2002 - 2004
Department of Neurology, Mayo Clinic, Rochester, USA. 2003

References

Lack of founder haplotype for the rapsyn N88K mutation: N88K is an ancient founder mutation or arises from multiple founders. Ohno, K., Engel, A.G. J. Med. Genet. (2004) [Pubmed]
E-box mutations in the RAPSN promoter region in eight cases with congenital myasthenic syndrome. Ohno, K., Sadeh, M., Blatt, I., Brengman, J.M., Engel, A.G. Hum. Mol. Genet. (2003) [Pubmed]
A frameshifting mutation in CHRNE unmasks skipping of the preceding exon. Ohno, K., Milone, M., Shen, X.M., Engel, A.G. Hum. Mol. Genet. (2003) [Pubmed]
Congenital myasthenic syndromes: genetic defects of the neuromuscular junction. Ohno, K., Engel, A.G. Curr. Neurol. Neurosci. Rep (2002) [Pubmed]