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Annu Rev Biophys 41:227246 Valds-Mas R, Gutirrez-Fernndez A, Gmez J, Coto E, Astudillo A, Puente DA, Reguero JR, lvarez V, Mors C, Len D, Martn M, Puente XS, Lpez-Otn C (2014) Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

High doses should always be supervised by a medical professional to ensure they do not cause unintended side effects for you or your baby

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Association between heterozygote Val92Met MC1R gene polymorphisms with incidence of melasma: a study of Javanese women population in Yogyakarta

Its primary role is to protect cells from damage caused by free radicals, toxins, and heavy metals