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

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Sara E. Mole

Department of Paediatrics

Royal Free and University College Medical School

University College London

The Rayne Institute

United Kingdom

[email]@ucl.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Paediatrics, Royal Free and University College Medical School, University College London, The Rayne Institute, United Kingdom. 1999 - 2004

References

  1. Neuronal ceroid lipofuscinoses (NCL). Mole, S.E. Eur. J. Paediatr. Neurol. (2006) [Pubmed]
  2. Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses. Mole, S.E., Williams, R.E., Goebel, H.H. Neurogenetics (2005) [Pubmed]
  3. The genetic spectrum of human neuronal ceroid-lipofuscinoses. Mole, S.E. Brain Pathol. (2004) [Pubmed]
  4. Neuronal ceroid lipofuscinoses (NCL). Mole, S. Eur. J. Paediatr. Neurol. (2004) [Pubmed]
  5. CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein. Mole, S.E., Michaux, G., Codlin, S., Wheeler, R.B., Sharp, J.D., Cutler, D.F. Exp. Cell Res. (2004) [Pubmed]
  6. Gene table: neuronal ceroid lipofuscinoses. Mole, S. Eur. J. Paediatr. Neurol. (2002) [Pubmed]
  7. Neuronal ceroid lipofuscinoses. Mole, S. Eur. J. Paediatr. Neurol. (2001) [Pubmed]
  8. New mutations in the neuronal ceroid lipofuscinosis genes. Mole, S.E., Zhong, N.A., Sarpong, A., Logan, W.P., Hofmann, S., Yi, W., Franken, P.F., van Diggelen, O.P., Breuning, M.H., Moroziewicz, D., Ju, W., Salonen, T., Holmberg, V., Järvelä, I., Taschner, P.E. Eur. J. Paediatr. Neurol. (2001) [Pubmed]
  9. Molecular basis of the neuronal ceroid lipofuscinoses: mutations in CLN1, CLN2, CLN3, and CLN5. Mole, S.E., Mitchison, H.M., Munroe, P.B. Hum. Mutat. (1999) [Pubmed]
 
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