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Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene.

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Bibliographic Details
Title: Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene.
Authors: Kim, Ka Young1, Heo, You Joung2, Ko, Jung Min3, Lee, Young Ah3, Shin, Choong Ho3, Ki, Chang Seok4, Lee, Yun Jeong3 yjlee103@snu.ac.kr
Source: BMC Endocrine Disorders. 4/15/2024, Vol. 24 Issue 1, p1-6. 6p.
Database: Academic Search Ultimate
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Description
ISSN:14726823
DOI:10.1186/s12902-024-01574-9