Regional difference of LDL receptor gene mutations in Japanese patients with familial hypercholesterolemia
β Scribed by Yu, W.X.; Nohara, A.; Inazu, A.; Koizumi, J.; Mabuchi, H.
- Book ID
- 121987050
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 115 KB
- Volume
- 151
- Category
- Article
- ISSN
- 0021-9150
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Communicated by Alec J. Jeffreys Familial hypercholesterolemia by usual definition reflects mutations of the LDL-receptor gene. Extensive molecular characterization of mutations ascertained mainly through homozygotes (the Dallas collection) has been presented by Hobbs et al. (Hum Mutat 1:445-466, 19
We used the denaturing gradient gel electrophoresis (DGGE) method to investigate 120 Japanese patients with familial hypercholesterolemia (FH) for mutations in the promoter region and the 18 exons and their flanking intron sequence of the low density lipoprotein (LDL) receptor gene. Fourteen aberran