Associated Papers
Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia.
Brandes D et al.
Hemasphere, 2023
37469802 (PubMed )
Supplement: hs9-7-e925-s001.xlsx › Table_S5_
Genetic analysis of the LRP10 gene in Chinese patients with Parkinson's disease.
Song N et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2023
Genetic and Epigenetic Constructs of Progressive Supranuclear Palsy.
Debnath M et al.
Annals of Neurosciences, 2022
Screening of LRP10 mutations in Parkinson's disease patients from Italy.
Manini A et al.
Parkinsonism & Related Disorders, 2021
LRP10 variants in progressive supranuclear palsy.
Vergouw LJM et al.
Neurobiology of Aging, 2020
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