Abstract
Background and Aims : FCS is an extremely rare genetic disease resulting in severe chylomicronaemia and high risk of recurrent pancreatitis in early childhood. Genes causing the disease include LPL, APOA5, APOC2, LMF1, and GPIHBP1.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
