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Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).
Hum Genet. 2018 Sep;137(9):753-768. doi: 10.1007/s00439-018-1929-5. Epub 2018 Aug 23.
Hum Genet. 2018.
PMID: 30167850
Free PMC article.
Severe neonatal seizures: From molecular diagnosis to precision therapy?
Milh M, Cacciagli P, Ravix C, Badens C, Lépine A, Villeneuve N, Villard L.
Milh M, et al. Among authors: ravix c.
Rev Neurol (Paris). 2016 Mar;172(3):171-3. doi: 10.1016/j.neurol.2016.02.005. Epub 2016 Mar 15.
Rev Neurol (Paris). 2016.
PMID: 26993565
Review.
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