Raymon Vijzelaar

3PUBLICATIONS
21CO-AUTHORS
OptometryNeurology and neuromuscular diseases
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Publications (3)

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|Jun 27, 2022
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy.

Bernd Wissinger, Britta Baumann, Elena Buena-Atienza

|Jun 25, 2021
SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral Sclerosis.

Jeroen W Bos, Ewout J N Groen, Renske I Wadman

|Jul 25, 2019
The frequency of SMN gene variants lacking exon 7 and 8 is highly population dependent.

Raymon Vijzelaar, Reinier Snetselaar, Martijn Clausen

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Frequent Collaborators

1 joint publications

Ewout J N Groen

1 joint publications

Bernd Wissinger

1 joint publications

Zeinab Ravesh

1 joint publications

Artur V Cideciyan

1 joint publications

Katarina Stingl

1 joint publications

Isabelle Audo

1 joint publications

Isabelle Meunier

1 joint publications

Beatrice Bocquet

1 joint publications

Elias I Traboulsi

1 joint publications

Alison J Hardcastle

Frequent Collaborators

1 joint publications

Ewout J N Groen

1 joint publications

Bernd Wissinger

1 joint publications

Zeinab Ravesh

1 joint publications

Artur V Cideciyan

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