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Author/Creator Oz Levi, D.

1. Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin. (January 2018)

Authors:
Heimer, G.; Eyal, E.; Zhu, X.; Ruzzo, E.K.; Marek-Yagel, D.; Sagiv, Doron; Anikster, Y.; Reznik-Wolf, H.; Pras, E.; Oz Levi, D.; Lancet, D.; Ben-Zeev, B.; Nissenkorn, A.
Journal:
European journal of paediatric neurology
Issue:
Volume 22:Number 1(2018:Jan.)
Page Start:
93
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum. (28th July 2015)

Authors:
Heimer, G.; Marek‐Yagel, D.; Eyal, E.; Barel, O.; Oz Levi, D.; Hoffmann, C.; Ruzzo, E.K.; Ganelin‐Cohen, E.; Lancet, D.; Pras, E.; Rechavi, G.; Nissenkorn, A.; Anikster, Y.; Goldstein, D.B.; Ben Zeev, B.
Journal:
Clinical genetics
Issue:
Volume 88:Number 4(2015:Oct.)
Page Start:
327
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗