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Page 1
Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders.
Int J Mol Sci. 2021 Mar 10;22(6):2824. doi: 10.3390/ijms22062824.
Int J Mol Sci. 2021.
PMID: 33802230
Free PMC article.
Prospective evaluation of NGS-based sequencing in epilepsy patients: results of seven NASGE-associated diagnostic laboratories.
Witzel MGW, Gebhard C, Wenzel S, Kleier S, Eichhorn B, Lorenz P, von der Heyden L, Kuhn M, Luedeke M, Döcker M, Jüngling J, Schulte B, Hörtnagel K, Glaubitz R, Knippenberger S, Teubert A, Abicht A, Neuhann TM.
Witzel MGW, et al. Among authors: jungling j.
Front Neurol. 2023 Dec 6;14:1276238. doi: 10.3389/fneur.2023.1276238. eCollection 2023.
Front Neurol. 2023.
PMID: 38125836
Free PMC article.
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Case Report of a Juvenile Patient with Autism Spectrum Disorder with a Novel Combination of Copy Number Variants in ADGRL3 (LPHN3) and Two Pseudogenes.
Maurer MH, Kohler A, Hudemann M, Jüngling J, Biskup S, Menzel M.
Maurer MH, et al. Among authors: jungling j.
Appl Clin Genet. 2022 Sep 2;15:125-131. doi: 10.2147/TACG.S361239. eCollection 2022.
Appl Clin Genet. 2022.
PMID: 36082049
Free PMC article.
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SYNGAP1 Mutation in Focal and Generalized Epilepsy: A Literature Overview and A Case Report with Special Aspects of the EEG.
von Stülpnagel C, Funke C, Haberl C, Hörtnagel K, Jüngling J, Weber YG, Staudt M, Kluger G.
von Stülpnagel C, et al. Among authors: jungling j.
Neuropediatrics. 2015 Aug;46(4):287-91. doi: 10.1055/s-0035-1554098. Epub 2015 Jun 25.
Neuropediatrics. 2015.
PMID: 26110312
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