5,10-Methylenetetrahydrofolate Reductase Deficiency and Myoclonic Epilepsy
By: J Gordon Millichap and John J Millichap
References
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- Lossos A Teltsh O Milman T Meiner V Rozen R Leclerc D Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegia JAMA Neurol 2014 Jul 1 71 7 901 4 10.1001/jamaneurol.2014.116 24797679
- Zupanc ML Legros B Progressive myoclonic epilepsy Cerebellum 2004 3 3 156 71 10.1080/14734220410035356 15543806
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DOI: https://doi.org/10.15844/pedneurbriefs-28-9-3 | Journal eISSN: 2166-6482
Language: English
Page range: 67 - 68
Published on: Sep 1, 2014
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2014 J Gordon Millichap, John J Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.