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DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndrome
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  1. Correspondence to:
 Forbes D Porter
 Heritable Disorders Branch, NICHD, NIH, DHHS, Bld. 10, Rm. 9S241, 10 Center Dr., Bethesda, MD 20892, USA; fdportermail.nih.gov
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Citation

Correa-Cerro LS, Wassif CA, Waye JS, et al
DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndrome

Publication history

  • Received May 12, 2004
  • Revised June 16, 2004
  • First published April 1, 2005.
Online issue publication 
April 01, 2005

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