Motor function impairment is an early sign of CLN3 disease
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Article Information
- Received August 1, 2018
- Accepted in final form March 4, 2019
- First Published June 10, 2019.
Article Versions
- Previous version (June 10, 2019 - 12:45).
- You are viewing the most recent version of this article.
Author Disclosures
- Willemijn F.E. Kuper, MD,
- Claudia van Alfen, MD,
- Linda van Eck, BSc,
- Barbara C.H. Huijgen, PhD,
- Edward E.S. Nieuwenhuis, MD, PhD,
- Marco van Brussel, PhD and
- Peter M. van Hasselt, MD, PhD
- Willemijn F.E. Kuper, MD,
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1) Beat Batten Foundation (non-profit). 2) Bartimeus foundation (non-profit). 3) Friends of the Wilhelmina Children's Hospital (non-profit)
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- Claudia van Alfen, MD,
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- Linda van Eck, BSc,
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- Barbara C.H. Huijgen, PhD,
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- Edward E.S. Nieuwenhuis, MD, PhD,
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- Marco van Brussel, PhD and
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- Peter M. van Hasselt, MD, PhD
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- From the Departments of Metabolic Diseases (W.F.E.K., P.M.v.H.), Pediatric Gastroenterology (E.E.S.N.), and Medical Physiology, Child Development and Exercise Center (M.v.B.), Wilhelmina Children's Hospital, University Medical Center Utrecht; Bartiméus Institute for the Visually Impaired (C.v.A., L.v.E.), Zeist and Doorn; and Center for Human Movement Sciences (B.C.H.H.), University Medical Center Groningen, University of Groningen, the Netherlands.
- Correspondence
Dr. van Hasselt p.vanhasselt{at}umcutrecht.nl
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