Apolipoprotein B gene mutation related to familial hypercholesterolemia in an Iranian population: With or without hypothyroidism

BACKGROUND: Familial hypercholesterolemia (FH) leads to elevated low-density lipoprotein cholesterol (LDL-C) levels in plasma. Mutations of its related gene; apolipoprotein B (APOB) is seen in about two percent of the patient with FH. Thyroid disease is usually part of the exclusion criteria for the...

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Detalles Bibliográficos
Autores principales: Vaseghi, Golnaz, Malakoutikhah, Zahra, Shafiee, Zahra, Gharipour, Mojgan, Shariati, Laleh, Sadeghian, Ladan, Khosravi, Elham, Javanmard, Shaghayegh Haghjooy, Pourmoghaddas, Ali, Laher, Ismail, Zarfeshani, Sonia, Sarrafzadegan, Nizal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607183/
https://www.ncbi.nlm.nih.gov/pubmed/34899932
http://dx.doi.org/10.4103/jrms.JRMS_970_19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607183/
https://www.ncbi.nlm.nih.gov/pubmed/34899932
http://dx.doi.org/10.4103/jrms.JRMS_970_19

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