Group Van Haaften, section Genetics

Research output

Research output per year 1997 2015 2016 2018 2019 2021 2023

• 64 Article
• 4 Meeting Abstract
• 2 Abstract
• 2 Comment/Letter to the editor
• 4 More
  • 2 Review article
  • 1 Editorial
  • 1 Letter

Research output per year

Research output per year

Search results

• 2016

  Correction: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability

  Lodder, E. M., De Nittis, P., Koopman, C. D., Wiszniewski, W., Moura de Souza, C. F., Lahrouchi, N., Guex, N., Napolioni, V., Tessadori, F., Beekman, L., Nannenberg, E. A., Boualla, L., Blom, N. A., de Graaff, W., Kamermans, M., Cocciadiferro, D., Malerba, N., Mandriani, B., Coban Akdemir, Z. H., Fish, R. J., & 13 othersEldomery, M. K., Ratbi, I., Wilde, A. A. M., de Boer, T., Simonds, W. F., Neerman-Arbez, M., Sutton, V. R., Kok, F., Lupski, J. R., Reymond, A., Bezzina, C. R., Bakkers, J. & Merla, G., 1 Sept 2016, In: American Journal of Human Genetics. 99, 3, p. 786

  Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review
• 2015

  Monocarboxylate transporter 1 deficiency and ketone utilization

  van Hasselt, P. M., Ferdinandusse, S. & van Haaften, G., 5 Feb 2015, In: New England Journal of Medicine. 372, 6, p. 578-579 2 p.

  Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

  Open Access

  File
  1 Downloads (Pure)