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2-Vinylpyridine | C7H7N | CID 7521 - PubChem

[DOI] [PMC free article] [PubMed] [Google Scholar] 166.Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

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How to Fix Low Cholesterol Correct Malabsorption If you have celiac disease, avoid gluten and work with a registered dietitian to design a nutrient-replete, gluten-free meal plan that corrects nutrient deficiencies while still allowing you to avoid sources of gliadin and glutenin