| dc.contributor.author | Oktay, Y | |
| dc.contributor.author | Gungor, S | |
| dc.contributor.author | Hiz, S | |
| dc.contributor.author | Yaramis, A | |
| dc.contributor.author | Aranguren-Ibanez, A | |
| dc.contributor.author | Yis, U | |
| dc.contributor.author | Sonmezler, E | |
| dc.contributor.author | Yilmaz, E | |
| dc.contributor.author | Ekinci, B | |
| dc.contributor.author | Aslan, M | |
| dc.contributor.author | Balaraju, S | |
| dc.contributor.author | Szabo, N | |
| dc.contributor.author | Laurie, S | |
| dc.contributor.author | Beltran, S | |
| dc.contributor.author | Hathazi, D | |
| dc.contributor.author | MacArthur, D | |
| dc.contributor.author | Roos, A | |
| dc.contributor.author | Lochmuller, H | |
| dc.contributor.author | Vernos, I | |
| dc.contributor.author | Horvath, R | |
| dc.date.accessioned | 2022-10-11T13:13:23Z | |
| dc.date.available | 2022-10-11T13:13:23Z | |
| dc.date.issued | 2020 | |
| dc.identifier.uri | http://hdl.handle.net/11616/75643 | |
| dc.source | EUROPEAN JOURNAL OF HUMAN GENETICS | |
| dc.title | A homozygous missense variant inTUBGCP2alter the g-tubulin ring complex | |
| dc.title | leading to abnormal cortical development, pontocerebellar atrophy and | |
| dc.title | altered myelination |
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