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SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype
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  1. Professor M Upadhyaya, Institute of Medical Genetics, Cardiff University, Heath Park, Cardiff CF14 4XN, UK; Upadhyaya{at}cardiff.ac.uk
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Citation

Spurlock G, Bennett E, Chuzhanova N, et al
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype

Publication history

  • Received December 5, 2008
  • Revised February 12, 2009
  • Accepted February 13, 2009
  • First published May 13, 2009.
Online issue publication 
July 01, 2009

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