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This ensures an accurate assessment of B12 status, the identification of any underlying conditions contributing to deficiency, and the development of an appropriate treatment plan
10.1093/gerona/glw043 57 FerrucciL.Gonzalez-FreireM.FabbriE.SimonsickE.TanakaT.MooreZ.et al
A sequence variation (I148M) in PNPLA3 associated with nonalcoholic fatty liver disease disrupts triglyceride hydrolysis
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