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Information Journal Paper

Title

FAMILIAL DEFECTIVE APOLIPORROTEIN B 100: FREQUENCY OF R3500Q MUTATION OF APOLIPOROTEIN B GENE IN IRANIAN HYPERCHOLESTEROLEMIC PATIENTS

Pages

  193-196

Abstract

FAMILIAL DEFECTIVE APOLIPOPROTEIN (apo) B 100 (FDB) causes early-onset coronary heart diseases (CHD). It is produced by R3500Q mutation of the apoB gene resulting in decreased binding of LDL to LDL receptor. We screened the apo B gene for R3500Q mutation in 130 hypercholesterolemic patients, among whom 30 patients met criteria of FAMILIAL HYPERCHOLESTEROLEMIA (FH). The prevalence of R3500Q allele in this patient population was 0%. To obtain better estimation of mutation frequency, a broad survey is needed.

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    APA: Copy

    FARDESFAHANI, P., MOHAMMADI TORBATI, P., KHATAMI, S., ZEYNALI, S., & TAGHIKHANI, M.. (2005). FAMILIAL DEFECTIVE APOLIPORROTEIN B 100: FREQUENCY OF R3500Q MUTATION OF APOLIPOROTEIN B GENE IN IRANIAN HYPERCHOLESTEROLEMIC PATIENTS. ACTA MEDICA IRANICA, 43(3), 193-196. SID. https://sid.ir/paper/277840/en

    Vancouver: Copy

    FARDESFAHANI P., MOHAMMADI TORBATI P., KHATAMI S., ZEYNALI S., TAGHIKHANI M.. FAMILIAL DEFECTIVE APOLIPORROTEIN B 100: FREQUENCY OF R3500Q MUTATION OF APOLIPOROTEIN B GENE IN IRANIAN HYPERCHOLESTEROLEMIC PATIENTS. ACTA MEDICA IRANICA[Internet]. 2005;43(3):193-196. Available from: https://sid.ir/paper/277840/en

    IEEE: Copy

    P. FARDESFAHANI, P. MOHAMMADI TORBATI, S. KHATAMI, S. ZEYNALI, and M. TAGHIKHANI, “FAMILIAL DEFECTIVE APOLIPORROTEIN B 100: FREQUENCY OF R3500Q MUTATION OF APOLIPOROTEIN B GENE IN IRANIAN HYPERCHOLESTEROLEMIC PATIENTS,” ACTA MEDICA IRANICA, vol. 43, no. 3, pp. 193–196, 2005, [Online]. Available: https://sid.ir/paper/277840/en

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