Long-term follow-up in two siblings with pyridoxine-dependent seizures associated with a novel ALDH7A1 mutation. [electronic resource]
- European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society Nov 2011
- 547-50 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
1532-2130
10.1016/j.ejpn.2011.05.011 doi
Adolescent Aldehyde Dehydrogenase--genetics Corpus Callosum--pathology Diffusion Magnetic Resonance Imaging Electroencephalography Epilepsy--drug therapy Female Genetic Association Studies Humans Longitudinal Studies Male Mutation--genetics Pyridoxine--therapeutic use Siblings Vitamin B Complex--therapeutic use