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

P.B. Munroe

Department of Pediatrics

University College London Medical School

The Rayne Institute

United Kingdom

[email]@ucl.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Pediatrics, University College London Medical School, The Rayne Institute, United Kingdom. 1997 - 1999

References

  1. Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome. Munroe, P.B., Olgunturk, R.O., Fryns, J.P., Van Maldergem, L., Ziereisen, F., Yuksel, B., Gardiner, R.M., Chung, E. Nat. Genet. (1999) [Pubmed]
  2. Spectrum of mutations in the Batten disease gene, CLN3. Munroe, P.B., Mitchison, H.M., O'Rawe, A.M., Anderson, J.W., Boustany, R.M., Lerner, T.J., Taschner, P.E., de Vos, N., Breuning, M.H., Gardiner, R.M., Mole, S.E. Am. J. Hum. Genet. (1997) [Pubmed]
 
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