Severe neurodevelopmental disease caused by a homozygous TLK2 variant

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	2022-09-22T08:28:08Z
dc.date.available	2022-09-22T08:28:08Z
dc.date.issued	2019
dc.identifier.uri	http://hdl.handle.net/11616/61689
dc.source	EUROPEAN JOURNAL OF HUMAN GENETICS
dc.title	Severe neurodevelopmental disease caused by a homozygous TLK2 variant

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