Article info
PDFDevelopmental defects
Original article
Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder
- Correspondence to Dr Donna M Martin, Departments of Pediatrics and Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA; donnamm{at}umich.edu
Citation
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
July 30, 2016
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