Skip to main content
Log in

β-Ureidopropionase deficiency: phenotype, genotype and protein structural consequences in 16 patients

  • Published:
Tijdschrift voor Kindergeneeskunde

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

van Kuilenburg, A., Dobritzsch, D., Meijer, J. et al. β-Ureidopropionase deficiency: phenotype, genotype and protein structural consequences in 16 patients. TIJDSCHR. KINDERGENEESKUNDE 81 (Suppl 1), 73–74 (2013). https://doi.org/10.1007/s12456-013-0071-5

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12456-013-0071-5

Navigation