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Author/Creator Koenekoop, R K

1. A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population. Issue 9 (5th September 2003)

Authors:
Yzer, S; van den Born, L I; Schuil, J; Kroes, H Y; van Genderen, M M; Boonstra, F N; van den Helm, B; Brunner, H G; Koenekoop, R K; Cremers, F P M
Journal:
Journal of medical genetics
Issue:
Volume 40:Issue 9(2003)
Page Start:
709
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. WDR19: An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior‐Loken syndrome. (9th July 2013)

Authors:
Coussa, R G; Otto, E A; Gee, H‐Y; Arthurs, P; Ren, H; Lopez, I; Keser, V; Fu, Q; Faingold, R; Khan, A; Schwartzentruber, J; Majewski, J; Hildebrandt, F; Koenekoop, R K
Journal:
Clinical genetics
Issue:
Volume 84:Number 2(2013:Aug.)
Page Start:
150
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗