Novel compound heterozygous mutations for lipoprotein lipase deficiency: a G-to-T transversion at the first position of exon 5 causing G154V missense mutation and a 5′ splice site mutation of intron 8-Reference-Cited by-同舟云学术

Novel compound heterozygous mutations for lipoprotein lipase deficiency: a G-to-T transversion at the first position of exon 5 causing G154V missense mutation and a 5′ splice site mutation of intron 8

Published:2001-07 Issue:7 Volume:42 Page:1072-1081
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Ikeda Yasuyuki,Takagi Atsuko,Nakata Yuusei,Sera Yasuhiko,Hyoudou Sumio,Hamamoto Kazuko,Nishi Yoshikazu,Yamamoto Akira

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference34 articles.

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5. Human genes involved in lipolysis of plasma lipoproteins: mapping of loci for lipoprotein lipase to 8p22 and hepatic lipase to 15q21;Sparkes;Genomics,1987

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