Associated Papers
Common and rare variants in patients with early onset drusen maculopathy.
de Breuk A et al.
Clinical Genetics, 2022
36053979 (PubMed )
Supplement: CGE-102-414-s009.xlsx › Blad1
Dementia-related genetic variants in an Italian population of early-onset Alzheimer's disease.
Bartoletti-Stella A et al.
Frontiers in Aging Neuroscience, 2022
Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients.
Hebert L et al.
Plos One, 2020
32970752 (PubMed )
Supplement: pone.0239083.s007.xlsx › S7_Table
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