Estela Rubio Gozalbo

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2016

Erratum to: ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies
Morava, E., Tiemes, V., Thiel, C., Seta, N., de Lonlay, P., de Klerk, H., Mulder, M., Rubio-Gozalbo, E., Visser, G., van Hasselt, P., Horovitz, D. D. G., Moura de Souza, C. F., Schwartz, I. V. D., Green, A., Al-Owain, M., Uziel, G., Sigaudy, S., Chabrol, B., van Spronsen, F-J., Steinert, M., & 11 othersKomini, E., Wurm, D., Bevot, A., Ayadi, A., Huijben, K., Dercksen, M., Witters, P., Jaeken, J., Matthijs, G., Lefeber, D. J. & Wevers, R. A., Sept 2016, In: Journal of Inherited Metabolic Disease. 39, 5, p. 759-759
Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic
2020
Correction to: Classical galactosemia: neuropsychological and psychosocial functioning beyond intellectual abilities (vol 15, 42, 2020)
Welsink-Karssies, M. M., Oostrom, K. J., Hermans, M. E., Hollak, C. E. M., Janssen, M. C. H., Langendonk, J. G., Oussoren, E., Rubio Gozalbo, M. E., de Vries, M., Geurtsen, G. J. & Bosch, A. M., 7 Sept 2020, In: Orphanet Journal of Rare Diseases. 15, 1, 4 p., 238.
Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

Open Access

Research output