Novel mutations identification in exon 4 of LDLR gene in patients with moderate hypercholesterolemia in a venezuelan population

Article

Abstract: Familial hypercholesterolemia (FH) is an autosomal dominant disease characterized by increase in low

Palabras claves:

Coronary artery disease, Familial hypercholesterolemia, Frameshift mutations, LDL-receptor, PCR-SSCP

Autores:

Arráiz N., Borjas L., Carem Prieto, Mujica E., Reyes F., Reyna-Villasmil N., Rondón N., Solís E., Valmore Bermúdez, Velasco M.

Fuentes:

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