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  • Phenotypic variability among patients with hyperornithinaemia–hyperammonaemia–homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15

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Phenotypic variability among patients with hyperornithinaemia–hyperammonaemia–homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15

Authors

  1. Grant A Mitchell, Division of Medical Genetics, CHU Sainte-Justine, 3175 Côte Sainte-Catherine, Montréal, Québec, H3T 1C5, Canada; grant.mitchell{at}recherche-ste-justine.qc.ca
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Citation

Debray F, Lambert M, Lemieux B, et al
Phenotypic variability among patients with hyperornithinaemia–hyperammonaemia–homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15
Journal of Medical Genetics 2008;45:759-764.

Publication history

  • Received March 18, 2008
  • Revised June 18, 2008
  • Accepted July 1, 2008
  • First published October 31, 2008.
Online issue publication 
April 27, 2016

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2008 BMJ Publishing Group Ltd