PuSH - Publication Server of Helmholtz Zentrum München

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1.
Wagner, M. et al.: Biallelic mutations in SLC1A2; an additional mode of inheritance for SLC1A2-related epilepsy. Neuropediatrics 49, 59-62 (2018)
2.
Baumeister, F.A.M.* ; Auer, D.P.* ; Hörtnagel, K. ; Freisinger, P.* & Meitinger, T.: The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome. Neuropediatrics 36, 221-222 (2005)