Cite
Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency
MLA
Kristin Ørstavik, et al. “Novel Mutations in the HADHB Gene Causing a Mild Phenotype of Mitochondrial Trifunctional Protein (MTP) Deficiency.” JIMD Reports, vol. 63, no. 3, May 2022, pp. 193–98. EBSCOhost, https://doi.org/10.1002/jmd2.12276.
APA
Kristin Ørstavik, Kjell Arne Arntzen, Per Mathisen, Paul Hoff Backe, Trine Tangeraas, Magnhild Rasmussen, Erle Kristensen, Marijke Van Ghelue, Christoffer Jonsrud, & Yngve Thomas Bliksrud. (2022). Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency. JIMD Reports, 63(3), 193–198. https://doi.org/10.1002/jmd2.12276
Chicago
Kristin Ørstavik, Kjell Arne Arntzen, Per Mathisen, Paul Hoff Backe, Trine Tangeraas, Magnhild Rasmussen, Erle Kristensen, Marijke Van Ghelue, Christoffer Jonsrud, and Yngve Thomas Bliksrud. 2022. “Novel Mutations in the HADHB Gene Causing a Mild Phenotype of Mitochondrial Trifunctional Protein (MTP) Deficiency.” JIMD Reports 63 (3): 193–98. doi:10.1002/jmd2.12276.