Pilar Mozas
Biographic Data
| ID | 4091513 |
|---|---|
| NAME | Pilar Mozas |
| GIVEN NAMES | Pilar |
| FAMILY NAME | Mozas |
| SIGNATURE | MOZAS P |
| VERIFIED | No |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 1 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2005 |
| LATEST PUBLICATION YEAR | 2005 |
| H-INDEX | 0 |
Screening of Apob Gene Mutations in Subjects with Clinical Diagnosis of Familial Hypercholesterolemia
Monogenic hypercholesterolemia is a group of lipid disorders, most of which have autosomal dominant transmission. Familial defective apoB (FDB) resulting from mutations in the APOB gene is a well-recognized cause of autosomal dominant monogenic hypercholesterolemia (ADMH). However, the frequency of FDB among patients with ADMH is not well established. The aim of our research was to screen for mutations responsible for FDB in subjects with a clini…
No prominent works on this page.
Screening of Apob Gene Mutations in Subjects with Clinical Diagnosis of Familial Hypercholesterolemia
Monogenic hypercholesterolemia is a group of lipid disorders, most of which have autosomal dominant transmission. Familial defective apoB (FDB) resulting from mutations in the APOB gene is a well-recognized cause of autosomal dominant monogenic hypercholesterolemia (ADMH). However, the frequency of FDB among patients with ADMH is not well established. The aim of our research was to screen for mutations responsible for FDB in subjects with a clini…
Apolipoprotein B (1 work) · Biology (1 work) · Cholesterol (1 work) · Cholesterol and Lipid Metabolism (1 work) · Diabetes, Cardiovascular Risks, and Lipoproteins (1 work) · Endocrinology (1 work) · Endocrinology (1 work) · Familial hypercholesterolemia (1 work) · Gene (1 work) · Gene mutation (1 work)