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Vanishing white matter disease with a novel EIF2B5 mutation..:
Bektaş, Gonca
;
Yeşil, Gözde
;
Özkan, Melis Ulak
...
Clinical Neurology and Neurosurgery. 171 (2018) - p. 190-193 , 2018
Link:
https://doi.org/10.1016/j.clineuro.2018.06.023
RT Journal T1
Vanishing white matter disease with a novel EIF2B5 mutation: A 10-year follow-up
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.clineuro.2018.06.023&Exemplar=1&LAN=DE A1 Bektaş, Gonca A1 Yeşil, Gözde A1 Özkan, Melis Ulak A1 Yıldız, Edibe Pembegül A1 Uzunhan, Tuğçe Aksu A1 Çalışkan, Mine PB Elsevier BV YR 2018 SN 0303-8467 JF Clinical Neurology and Neurosurgery VO 171 SP 190 OP 193 LK http://dx.doi.org/https://doi.org/10.1016/j.clineuro.2018.06.023 DO https://doi.org/10.1016/j.clineuro.2018.06.023 SF ELIB - SuUB Bremen
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