Genetic Variation at a Splicing Branch Point in Intron 9 of the Low Density Lipoprotein (LDL)-Receptor Gene: A Rare Mutation that Disrupts mRNA Splicing in a Patient with Familial Hypercholesterolaemia and a Common Polymorphism.

Autor: Webb, Julie C., Patel, Dilip D., Shoulders, Carol C., Knight, Brian L., Soutar, Anne K.
Zdroj: Human Molecular Genetics; Sep1996, Vol. 5 Issue 9, p1325-1331, 7p
Databáze: Complementary Index