You are here

  • Home
  • Archive
  • Volume 15, Issue 4
  • Transient infantile hypertriglyceridaemia due to homozygous mutation in GPD1 presenting in childhood with hepatic adenoma

Citation Tools

Article menu
Download PDFPDF
Case Reports: Rare disease
Transient infantile hypertriglyceridaemia due to homozygous mutation in GPD1 presenting in childhood with hepatic adenoma

Download to a citation manager

Download the citation for this article by clicking on one of the following citation managers:

Cite this article as:
Kumar K, Malhotra S, Sibal A
Transient infantile hypertriglyceridaemia due to homozygous mutation in GPD1 presenting in childhood with hepatic adenoma
BMJ Case Reports CP 2022;15:e248801.