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Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia
- Correspondence to: Dr L Villard, INSERM U491, Faculty of Medecine La Timone, 27 Bd Jean Moulin, 13385 Marseille, France; laurent.villard{at}medecine.univ-mrs.fr
Citation
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia
Publication history
- First published June 1, 2003.
Online issue publication
April 27, 2016
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Copyright 2003 Journal of Medical Genetics