Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia
✍ Scribed by K Brusgaard; P Jordan; H Hansen; AB Hansen; M Hørder
- Book ID
- 110888170
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 110 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0009-9163
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## Communicated by Mark H. Paalman Mutations underlying FH in Spain are largely unknown because only a few and limited surveys have been carried out on Spanish FH patients up to now. To gain information on this issue, we have analysed a group of 113 unrelated Spanish FH patients from an eastern ar
## Abstract We performed genetic analysis in 55 patients with clinical features of possible type IIa hypercholesterolemia and 76 normolipemic healthy subjects for mutations and polymorphisms in the low‐density lipoprotein (LDL) receptor (LDLR), apolipoprotein B‐100 (APOB), apolipoprotein E (APOE),