Associated Papers
Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients.
Pennisi EM et al.
Orphanet Journal of Rare Diseases, 2017
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene.
Fiorillo C et al.
Biochemical and Biophysical Research Communications, 2013
Select a paper to view details