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

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W. Lissens

Center for Medical Genetics

University Hospital of the Dutch-speaking Brussels Free University

Belgium

[email]@az.vub.ac.be

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Affiliations

Center for Medical Genetics, University Hospital of the Dutch-speaking Brussels Free University, Belgium. 1999 - 2000
Department of Paediatric Neurology, University Hospital, Vrije Universiteit Brussel, Brussels, Belgium. 1999

References

Mutations in the X-linked pyruvate dehydrogenase (E1) alpha subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency. Lissens, W., De Meirleir, L., Seneca, S., Liebaers, I., Brown, G.K., Brown, R.M., Ito, M., Naito, E., Kuroda, Y., Kerr, D.S., Wexler, I.D., Patel, M.S., Robinson, B.H., Seyda, A. Hum. Mutat. (2000) [Pubmed]
Molecular analysis of the cystic fibrosis gene reveals a high frequency of the intron 8 splice variant 5T in Egyptian males with congenital bilateral absence of the vas deferens. Lissens, W., Mahmoud, K.Z., El-Gindi, E., Abdel-Sattar, A., Seneca, S., Van Steirteghem, A., Liebaers, I. Mol. Hum. Reprod. (1999) [Pubmed]
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha gene. Lissens, W., Vreken, P., Barth, P.G., Wijburg, F.A., Ruitenbeek, W., Wanders, R.J., Seneca, S., Liebaers, I., De Meirleir, L. Eur. J. Pediatr. (1999) [Pubmed]