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Letter
WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype

Authors

  1. Correspondence to Dr Fowzan S Alkuraya, Department of Genetics, King Faisal Specialist Hospital & Research Center, Takhassousi Rd, Riyadh 11211, Saudi Arabia;FAlKuraya@kfshrc.edu.sa
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Citation

Faqeih E, Shaheen R, Alkuraya FS
WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype

Publication history

  • Received April 15, 2013
  • Accepted April 16, 2013
  • First published May 24, 2013.
Online issue publication 
June 11, 2013

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