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SCN2A mutation in an infant with Ohtahara syndrome and neuroimaging findings: expanding the phenotype of neuronal migration disorders
Vlachou, Victoria, Larsen, Line, Pavlidou, Efterpi, Ismayilova, Naila, Mazarakis, N. D., Pantazi, Mantha, Mankad, Kshitij, Kinali, MariaVolume:
98
Langue:
english
Journal:
Journal of Genetics
DOI:
10.1007/s12041-019-1104-3
Date:
June, 2019
Fichier:
PDF, 638 KB
english, 2019