| dc.contributor.author | Topf, A | |
| dc.contributor.author | Oktay, Y | |
| dc.contributor.author | Balaraju, S | |
| dc.contributor.author | Yilmaz, E | |
| dc.contributor.author | Sonmezler, E | |
| dc.contributor.author | Yis, U | |
| dc.contributor.author | Laurie, S | |
| dc.contributor.author | Thompson, R | |
| dc.contributor.author | Roos, A | |
| dc.contributor.author | MacArthur, DG | |
| dc.contributor.author | Yaramis, A | |
| dc.contributor.author | Gungor, S | |
| dc.contributor.author | Lochmuller, H | |
| dc.contributor.author | Hiz, S | |
| dc.contributor.author | Horvath, R | |
| dc.date.accessioned | 2022-10-11T13:33:22Z | |
| dc.date.available | 2022-10-11T13:33:22Z | |
| dc.date.issued | 2019 | |
| dc.identifier.uri | http://hdl.handle.net/11616/76383 | |
| dc.source | EUROPEAN JOURNAL OF HUMAN GENETICS | |
| dc.title | Severe neurodevelopmental disease caused by a homozygous TLK2 variant |
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