Horinishi A

References (2)

Title : A novel complex deletion-insertion mutation mediated by Alu repetitive elements leads to lipoprotein lipase deficiency - Okubo_2007_Mol.Genet.Metab_92_229
Author(s) : Okubo M , Horinishi A , Saito M , Ebara T , Endo Y , Kaku K , Murase T , Eto M
Ref : Mol Genet Metab , 92 :229 , 2007
Abstract : Okubo_2007_Mol.Genet.Metab_92_229
ESTHER : Okubo_2007_Mol.Genet.Metab_92_229
PubMedSearch : Okubo_2007_Mol.Genet.Metab_92_229
PubMedID: 17706445

Title : Detection of a new compound heterozygote (del G916\/G1401A) for lipoprotein lipase deficiency and a comparative haplotype analysis of the mutant lipoprotein lipase gene from Japanese patients -
Author(s) : Okubo M , Inoue S , Horinishi A , Ogihara T , Kaneko K , Gotoda T , Yamada N , Murase T
Ref : Atherosclerosis , 144 :443 , 1999
PubMedID: 10407506