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

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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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  Data: Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene.
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  Data: <searchLink fieldCode="AR" term="%22Kim%2C+Ka+Young%22">Kim, Ka Young</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Heo%2C+You+Joung%22">Heo, You Joung</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Ko%2C+Jung+Min%22">Ko, Jung Min</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Lee%2C+Young+Ah%22">Lee, Young Ah</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Shin%2C+Choong+Ho%22">Shin, Choong Ho</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Ki%2C+Chang+Seok%22">Ki, Chang Seok</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Lee%2C+Yun+Jeong%22">Lee, Yun Jeong</searchLink><relatesTo>3</relatesTo><i> yjlee103@snu.ac.kr</i>
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  Data: <searchLink fieldCode="JN" term="%22BMC+Endocrine+Disorders%22">BMC Endocrine Disorders</searchLink>. 4/15/2024, Vol. 24 Issue 1, p1-6. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=176609860
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      – Type: doi
        Value: 10.1186/s12902-024-01574-9
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        Text: English
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            NameFull: Kim, Ka Young
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            NameFull: Heo, You Joung
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              Text: 4/15/2024
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              Y: 2024
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