Associated Papers
Exome sequencing reveals a rare damaging variant in GRIN2C in familial late-onset Alzheimer's disease.
Rubino E et al.
Alzheimer's Research & Therapy, 2025
39810256 (PubMed )
Supplement: 13195_2024_1661_MOESM2_ESM.xlsx › Suppl._Table_2
Hereditary Hemochromatosis Caused by SUGP2 and DENND3 Mutation in China: A Case Report.
Qiu H et al.
Clinical Case Reports, 2024
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