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A 1-month-old infant with chylomicronemia due to GPIHBP1 gene mutation treated by plasmapheresis
Mo Kyung Jung, Juhyun Jin, Hyun Ok Kim, Ahreum Kwon, Hyun Wook Chae, Seok Jin Kang, Duk Hee Kim, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2017;22(1):68-71.   Published online March 31, 2017
DOI: https://doi.org/10.6065/apem.2017.22.1.68

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A 1-month-old infant with chylomicronemia due to GPIHBP1 gene mutation treated by plasmapheresis
Annals of Pediatric Endocrinology & Metabolism. 2017;22(1):68   Crossref logo
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