Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to Therapy
Author:
Funder
National Institute for Medical Research Development
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12031-022-01993-0.pdf
Reference33 articles.
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4. Chang A, Ruiz‐Lopez M, Slow E, Tarnopolsky M, Lang AE, Munhoz RP (2018) ADCK3‐related coenzyme Q10 deficiency: a potentially treatable genetic disease 5:635–639
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