| Title : Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene - Kim_2024_BMC.Endocr.Disord_24_47 |
| Author(s) : Kim KY , Heo YJ , Ko JM , Lee YA , Shin CH , Ki CS , Lee YJ |
| Ref : BMC Endocr Disord , 24 :47 , 2024 |
| Abstract : |
| PubMedSearch : Kim_2024_BMC.Endocr.Disord_24_47 |
| PubMedID: 38622573 |
| Title : Analysis of intrapatient heterogeneity uncovers the microevolution of Middle East respiratory syndrome coronavirus - Park_2016_Cold.Spring.Harb.Mol.Case.Stud_2_a001214 |
| Author(s) : Park D , Huh HJ , Kim YJ , Son DS , Jeon HJ , Im EH , Kim JW , Lee NY , Kang ES , Kang CI , Chung DR , Ahn JH , Peck KR , Choi SS , Ki CS , Park WY |
| Ref : Cold Spring Harb Mol Case Stud , 2 :a001214 , 2016 |
| Abstract : |
| PubMedSearch : Park_2016_Cold.Spring.Harb.Mol.Case.Stud_2_a001214 |
| PubMedID: 27900364 |
| Title : No association between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset Alzheimer's disease - Ki_1999_Am.J.Med.Genet_88_113 |
| Author(s) : Ki CS , Na DL , Kim JW , Kim HJ , Kim DK , Yoon BK |
| Ref : American Journal of Medicine Genet , 88 :113 , 1999 |
| Abstract : |
| PubMedSearch : Ki_1999_Am.J.Med.Genet_88_113 |
| PubMedID: 10206226 |