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C.J. Wilson

Metabolic Unit

Great Ormond Street Hospital for Children

Great Ormond Street

London WC1N 3JH

UK

[email]@yahoo.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Metabolic Unit, Great Ormond Street Hospital for Children, Great Ormond Street, London WC1N 3JH, UK. 1999 - 2000

References

  1. Autosomal recessive osteopetrosis: diagnosis, management, and outcome. Wilson, C.J., Vellodi, A. Arch. Dis. Child. (2000) [Pubmed]
  2. Phenylalanine supplementation improves the phenylalanine profile in tyrosinaemia. Wilson, C.J., Van Wyk, K.G., Leonard, J.V., Clayton, P.T. J. Inherit. Metab. Dis. (2000) [Pubmed]
  3. Mitochondrial DNA point mutation T9176C in Leigh syndrome. Wilson, C.J., Wood, N.W., Leonard, J.V., Surtees, R., Rahman, S. J. Child Neurol. (2000) [Pubmed]
  4. Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis. Wilson, C.J., Champion, M.P., Collins, J.E., Clayton, P.T., Leonard, J.V. Arch. Dis. Child. (1999) [Pubmed]
 
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