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The UGT1A mutation characteristic of Gilbert syndrome is associated with a much higher risk for NNJ and kernicterus in G6PD-deficient babies

First, this article reviews non-tumour diseases and conditions related to the Wnt/-catenin signalling pathway, such as hair loss, pigment disorders, wound healing, bone diseases, neurodegenerative diseases, and chronic obstructive pulmonary diseases

50 The consistent findings may be due to the fact that L-carnitine is a nonessential amino acid, which the body can synthesize from other amino acids in presence of other micronutrients

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