Frequency and significance of rare LIPA variants associated with lysosomal acid lipase deficiency in metabolic dysfunction–associated steatotic liver disease: Results from the Nonalcoholic Steatohepatitis Clinical Research Network

Jean P. Molleston receives research funding from AbbVie, Albireo, Gilead, Shire/Mirum, and Madrigal. The remaining authors declare no conflict of interest. All study phenotype data and Biosamples are stored at the NIDDK Central Repository (https://repository.niddk.nih.gov/home/). Interested investigators should go to the website and complete the request forms and agreements to use the study data and/or request biospecimens for each NASH CRN study used in this manuscript. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.