Article info

Original article
Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder
  1. Correspondence to Dr Donna M Martin, Departments of Pediatrics and Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA; donnamm{at}umich.edu
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Citation

Bedoyan JK, Schaibley VM, Peng W, et al
Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder

Publication history

  • Received October 18, 2011
  • Revised March 22, 2012
  • Accepted March 23, 2012
  • First published May 11, 2012.
Online issue publication 
May 11, 2012
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