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Description
with 12 studies with a total number of 1423 randomized participants [52]
Mutations in CPT1 can cause carnitine palmitoyltransferase I (CPT I) deficiency, which is an autosomal recessive genetic condition (need two copies of the mutation)
Vitamin E-supplementation protect chromium (VI)-induced spermatogenic and steroidogenic disorders in testicular tissues of rats
Fine-tuning of GPCR activity by receptor-interacting proteins
