Αρχειοθήκη ιστολογίου

Δευτέρα 8 Οκτωβρίου 2018

A novel SLC1A4 homozygous mutation causing congenital microcephaly, epileptic encephalopathy and spastic tetraparesis: a video-EEG and tractography - case study

Pironti, E; Salpietro, V; Cucinotta, F; Granata, F; Mormina, E; Efthymiou, S; Scuderi, C; ... Di Rosa, G; + view all Pironti, E; Salpietro, V; Cucinotta, F; Granata, F; Mormina, E; Efthymiou, S; Scuderi, C; Gagliano, A; Houlden, H; Di Rosa, G; - view fewer (2018) A novel SLC1A4 homozygous mutation causing congenital microcephaly, epileptic encephalopathy and spastic tetraparesis: a video-EEG and tractography - case study. Journal of Neurogenetics 10.1080/01677063.2018.1476510 . (In press).

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