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

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Kenjiro Kosaki

Department of Pediatrics

Keio University School of Medicine

Tokyo

Japan

[email]@med.keio.ac.jp

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Affiliation

Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan. 2002

References

A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: differential role of the polyalanine tract in the development of the ovary and the eyelid. Kosaki, K., Ogata, T., Kosaki, R., Sato, S., Matsuo, N. Ophthalmic Genet. (2002) [Pubmed]