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5. Identification of rare diseases by screening a population selected on the basis of routine pathology results-the PATHFINDER project: lysosomal acid lipase/cholesteryl ester storage disease substudy. Reynolds TM; Mewies C; Hamilton J; Wierzbicki AS; J Clin Pathol; 2018 Jul; 71(7):608-613. PubMed ID: 29358478 [TBL] [Abstract][Full Text] [Related]
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19. [Wolman disease with novel mutation of LIPA gene in a Chinese infant]. Huang YL; Sheng HY; Zhao XY; Yu JK; Li L; Liu HS; Gu CM; He DM; Liu L Zhonghua Er Ke Za Zhi; 2012 Aug; 50(8):601-5. PubMed ID: 23158738 [TBL] [Abstract][Full Text] [Related]