Abstract
Lysosomal Acid Lipase deficiency (LAL D) is lysosomal metabolic genetic disease caused by mutation in LIPA gene which encodes for the LAL enzyme. It characterised by multiorganic damage, mostly liver...
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
