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Author/Creator van den Hout, Mirjam C.G.N.

1. A functional variant in the miR‐142 promoter modulating its expression and conferring risk of Alzheimer disease. Issue 11 (7th August 2019)

Authors:
Ghanbari, Mohsen; Munshi, Shashini T.; Ma, Buyun; Lendemeijer, Bas; Bansal, Sakshi; Adams, Hieab H.; Wang, Wenshi; Goth, Kerstin; Slump, Denise E.; van den Hout, Mirjam C.G.N.; van IJcken, Wilfred F.J.; Bellusci, Saverio; Pan, Qiuwei; Erkeland, Stefan J.; de Vrij, Femke M.S.; Kushner, Steven A.; ...
Journal:
Human mutation
Issue:
Volume 40:Issue 11(2019)
Page Start:
2131
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Paroxysmal exercise‐induced dystonia within the phenotypic spectrum of ECHS1 deficiency. Issue 7 (19th April 2016)

Authors:
Olgiati, Simone; Skorvanek, Matej; Quadri, Marialuisa; Minneboo, Michelle; Graafland, Josja; Breedveld, Guido J.; Bonte, Ramon; Ozgur, Zeliha; van den Hout, Mirjam C.G.N.; Schoonderwoerd, Kees; Verheijen, Frans W.; van IJcken, Wilfred F.J.; Chien, Hsin Fen; Barbosa, Egberto Reis; Chang, Hsiu‐Chen...
Journal:
Movement disorders
Issue:
Volume 31:Issue 7(2016)
Page Start:
1041
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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