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Author/Creator de Coo, I.F.M.

1. A clinical diagnostic algorithm for early onset cerebellar ataxia. (September 2019)

Authors:
Brandsma, R.; Verschuuren-Bemelmans, C.C.; Amrom, D.; Barisic, N.; Baxter, P.; Bertini, E.; Blumkin, L.; Brankovic-Sreckovic, V.; Brouwer, O.F.; Bürk, K.; Catsman-Berrevoets, C.E.; Craiu, D.; de Coo, I.F.M.; Gburek, J.; Kennedy, C.; de Koning, T.J.; Kremer, H.P.H.; Kumar, R.; Macaya, A.; Micalizz...
Journal:
European journal of paediatric neurology
Issue:
Volume 23:Number 5(2019:Sep.)
Page Start:
692
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect. Issue 1 (21st November 2017)

Authors:
Baertling, F.; Sánchez‐Caballero, L.; van den Brand, M.A.M.; Fung, C.‐W.; Chan, S.H.‐S.; Wong, V.C.‐N.; Hellebrekers, D.M.E.; de Coo, I.F.M.; Smeitink, J.A.M.; Rodenburg, R.J.T.; Nijtmans, L.G.J.
Journal:
Clinical genetics
Issue:
Volume 93:Issue 1(2018)
Page Start:
111
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗