J. Jüngling

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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

M. Maurer, S. Biskup, Anja Kohler, 2022, The application of clinical genetics.

TACG_A_361239 125..131

M. Maurer, S. Biskup, Anja Kohler, 2022 .

SYNGAP1 Mutation in Focal and Generalized Epilepsy: A Literature Overview and A Case Report with Special Aspects of the EEG

C. Funke, Y. Weber, M. Staudt, 2015, Neuropediatrics.

Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders

G. Rubboli, R. Møller, T. Bast, 2021, International journal of molecular sciences.