Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia

BACKGROUND: Familial hypercholesterolemia is a genetic disorder mainly caused by defects in the low-density lipoprotein receptor gene. Few and limited analyses of familial hypercholesterolemia have been performed in Malaysia, and the underlying mutations therefore remain largely unknown. We studied...

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Detalles Bibliográficos
Autores principales: Al-Khateeb, Alyaa, Zahri, Mohd K, Mohamed, Mohd S, Sasongko, Teguh H, Ibrahim, Suhairi, Yusof, Zurkurnai, Zilfalil, Bin A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3071311/
https://www.ncbi.nlm.nih.gov/pubmed/21418584
http://dx.doi.org/10.1186/1471-2350-12-40

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3071311/
https://www.ncbi.nlm.nih.gov/pubmed/21418584
http://dx.doi.org/10.1186/1471-2350-12-40

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