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27. [Lysosomal acid lipase deficiency. Overview of Czech patients]. Elleder M; Poupĕtová H; Ledvinová J; Hyánek J; Zeman J; Sýkora J; Stozický F; Chlumská A; Lohse P Cas Lek Cesk; 1999 Nov; 138(23):719-24. PubMed ID: 10746035 [TBL] [Abstract][Full Text] [Related]
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29. Mutations at the lysosomal acid cholesteryl ester hydrolase gene locus in Wolman disease. Anderson RA; Byrum RS; Coates PM; Sando GN Proc Natl Acad Sci U S A; 1994 Mar; 91(7):2718-22. PubMed ID: 8146180 [TBL] [Abstract][Full Text] [Related]
30. A Novel Mutation c.153 C>A in a Tunisian Girl With Wolman Disease and Unusual Presentation: Hemophagocytic Lymphohistiocytosis. Tinsa F; Ben Romdhane M; Boudabous H; Bel Hadj I; Brini I; Tebib N; Louati H; Bekri S; Boussetta K J Pediatr Hematol Oncol; 2019 Apr; 41(3):e193-e196. PubMed ID: 29702543 [TBL] [Abstract][Full Text] [Related]
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