Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia › Research Explorer

DOI

https://doi.org/10.1093/hmg/ddu218
Final published version

Sander M. Houten
Simone Denis
Heleen te Brinke
Aldo Jongejan
Antoine H. C. van Kampen
Edward J. Bradley
Frank Baas
Raoul C. M. Hennekam
David S. Millington
Sarah P. Young
Dianne M. Frazier
Muge Gucsavas-Calikoglu
Ronald J. A. Wanders

Original language	English
Pages (from-to)	5009-5016
Journal	Human molecular genetics
Volume	23
Issue number	18
DOIs	https://doi.org/10.1093/hmg/ddu218
Publication status	Published - 2014

ID: 2411710