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

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Andrea H. Németh

Wellcome Trust Centre for Human Genetics

Oxford OX3 7BN

United Kingdom

[email]@well.ox.ac.uk

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Affiliation

Wellcome Trust Centre for Human Genetics, Oxford OX3 7BN, United Kingdom. 2000 - 2002

References

The genetics of primary dystonias and related disorders. Németh, A.H. Brain (2002) [Pubmed]
Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34. Németh, A.H., Bochukova, E., Dunne, E., Huson, S.M., Elston, J., Hannan, M.A., Jackson, M., Chapman, C.J., Taylor, A.M. Am. J. Hum. Genet. (2000) [Pubmed]