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These studies indicate the potential of utilizing the de novo pathway, a less extensively studied pathway, as a therapeutic strategy for metabolic diseases Barth syndrome is a rare disease caused by mutations in the tafazzin gene encoding for cardiolipin (CL), a phospholipid specific for the mitochondria 303
Neurological function
Color:330 Medium
Assess for symptoms suggestive of B12 deficiency, such as fatigue, pallor, dizziness, exertional dyspnea, palpitations, glossitis, numbness, paresthesia, balance disorders, memory impairment, or mood changes
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