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Author/Creator Hetterschijt, Lisette

1. KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome. Issue 1 (December 2015)

Authors:
Sanders, Anna; de Vrieze, Erik; Alazami, Anas; Alzahrani, Fatema; Malarkey, Erik; Sorusch, Nasrin; Tebbe, Lars; Kuhns, Stefanie; van Dam, Teunis; Alhashem, Amal; Tabarki, Brahim; Lu, Qianhao; Lambacher, Nils; Kennedy, Julie; Bowie, Rachel; Hetterschijt, Lisette; van Beersum, Sylvia; van Reeuwijk,...
Journal:
Genome biology
Issue:
Volume 16:Issue 1(2015)
Page Start:
1
Record Type:
Journal Article
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2. Missense mutations in the WD40 domain of AHI1 cause non-syndromic retinitis pigmentosa. Issue 9 (25th April 2017)

Authors:
Nguyen, Thanh-Minh T; Hull, Sarah; Roepman, Ronald; van den Born, L Ingeborgh; Oud, Machteld M; de Vrieze, Erik; Hetterschijt, Lisette; Letteboer, Stef J F; van Beersum, Sylvia E C; Blokland, Ellen A; Yntema, Helger G; Cremers, Frans P M; van der Zwaag, Paul A; Arno, Gavin; van Wijk, Erwin; Webst...
Journal:
Journal of medical genetics
Issue:
Volume 54:Issue 9(2017)
Page Start:
624
Record Type:
Journal Article
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3. Usherin defects lead to early-onset retinal dysfunction in zebrafish. (August 2018)

Authors:
Dona, Margo; Slijkerman, Ralph; Lerner, Kimberly; Broekman, Sanne; Wegner, Jeremy; Howat, Taylor; Peters, Theo; Hetterschijt, Lisette; Boon, Nanda; de Vrieze, Erik; Sorusch, Nasrin; Wolfrum, Uwe; Kremer, Hannie; Neuhauss, Stephan; Zang, Jingjing; Kamermans, Maarten; Westerfield, Monte; Phillips, ...
Journal:
Experimental eye research
Issue:
Volume 173(2018)
Page Start:
148
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗