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Original article
Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene

Authors

  1. Dr M Kobayashi, Department of Pediatrics, Hiroshima, University Graduate School of Biomedical Sciences, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8551 Japan; masak{at}hiroshima-u.ac.jp
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Citation

Ishikawa N, Okada S, Miki M, et al
Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene
Journal of Medical Genetics 2008;45:802-807.

Publication history

  • Received February 19, 2008
  • Revised June 17, 2008
  • Accepted June 19, 2008
  • First published July 8, 2008.
Online issue publication 
April 27, 2016

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2008 BMJ Publishing Group