Familial hypercholesterolemia (FH) is an autosomal dominant disorder mostly caused by mutations in the LDLR gene. Although the detection of functional mutations in the LDLR gene provides an unequivocal diagnosis of the FH condition, there are many variants whose pathogenicity is still unknown. The a
✦ LIBER ✦
Structural and Functional Characterization of the Aryl Hydrocarbon Receptor Ligand Binding Domain by Homology Modeling and Mutational Analysis†
✍ Scribed by Pandini, Alessandro; Denison, Michael S.; Song, Yujuan; Soshilov, Anatoly A.; Bonati, Laura
- Book ID
- 111951101
- Publisher
- American Chemical Society
- Year
- 2007
- Tongue
- English
- Weight
- 637 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0006-2960
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