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

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De novo mutation of the myelin Po gene in Déjérine-Sottas disease (hereditary motor and sensory neuropathy type III): two amino acid insertion after Asp 118.

[1]

References

  1. De novo mutation of the myelin Po gene in Déjérine-Sottas disease (hereditary motor and sensory neuropathy type III): two amino acid insertion after Asp 118. Ikegami, T., Nicholson, G., Ikeda, H., Ishida, A., Johnston, H., Wise, G., Ouvrier, R., Hayasaka, K. Hum. Mutat. (1998) [Pubmed]
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