A detailed Hapmap of the Sitosterolemia locus spanning 69 kb; differences between Caucasians and African-Americans

Autor: Hazard Starr E, Ahn Gwang-Sook, Pandit Bhaswati, Gordon Derek, Patel Shailendra B

Publikováno v: BMC Medical Genetics, Vol 7, Iss 1, p 13 (2006)

Abstract Background Sitosterolemia is an autosomal recessive disorder that maps to the sitosterolemia locus, STSL, on human chromosome 2p21. Two genes, ABCG5 and ABCG8, comprise the STSL and mutations in either cause sitosterolemia. ABCG5 and ABCG8 a

Externí odkaz: https://doaj.org/article/c37aaf1fc5a04f20977e913bfb3ca7b4

A detailed Hapmap of the Sitosterolemia locus spanning 69 kb; differences between Caucasians and African-Americans.

Autor: Pandit B; Division of Endocrinology, Diabetes and Medical Genetics, Medical University of South Carolina, STR 541, 114 Doughty Street, Charleston, SC 29403, USA. bhaswati.pandit@mssm.edu, Ahn GS, Hazard SE, Gordon D, Patel SB

Publikováno v: BMC medical genetics [BMC Med Genet] 2006 Feb 28; Vol. 7, pp. 13. Date of Electronic Publication: 2006 Feb 28.