Background: Heterozygous progranulin (GRN) mutations are an important cause of
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Vandevrede, L., Rojas, J. C., Wang, P., Heuer, H. W., Karydas, A. M., … Boxer, A. L. (2020). Lipid metabolism dysfunction in progranulin mutation carriers: Unbiased metabolomics reveals strong relationship to clinical status in FTLD. Alzheimer’s & Dementia, 16(S5). https://doi.org/10.1002/alz.046594
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