Familial hypercholesterolemia (FH) is a genetic disorder caused by numerous mutations in the low-density lipoprotein receptor (LDLR) gene. Mutational analyses of Indians in South Africa suggest the possibility of a high frequency of FH in India. This study aimed at identifying mutations in exons 3,
✦ LIBER ✦
Two founder mutations in the LDL receptor gene in Norwegian familial hypercholesterolemia subjects
✍ Scribed by Trond P. Leren; Kari Solberg; Olaug K. Rødningen; Serena Tonstad; Leiv Ose
- Book ID
- 118324604
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 768 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0021-9150
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