Onderzoek van de niet-ketotische hyperglycinaemie; een erfelijke stofwisselingsziekte.

Cornelis Jacob de Groot

Research output: ThesisThesis fully internal (DIV)

55 Downloads (Pure)

Abstract

The non-ketotic form of hyperglycinaemia is a rare disorder. Less than 20 cases have been published until now. In the Department of Paediatrics of the State University in Groningen we were able to observe five patients with this inborn error of metabolism.
Original languageDutch
QualificationDoctor of Philosophy
Supervisors/Advisors
  • JONXIS, JHP, Supervisor, External person
Publisher
Publication statusPublished - 1971

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