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1.
Charif, M.* et al.: Neurologic phenotypes associated with mutations in RTN4IP1 (OPA10) in children and young adults. JAMA Neurol. 75, 105-113 (2018)
2.
Karch, C.M.* et al.: Selective genetic overlap between amyotrophic lateral sclerosis and diseases of the frontotemporal dementia spectrum. JAMA Neurol. 75, 860-875 (2018)
3.
Sommerville, E.W.* et al.: Clinical features, molecular heterogeneity, and prognostic implications in YARS2-related mitochondrial myopathy. JAMA Neurol. 74, 686-694 (2017)
4.
Witoelar, A.W.* et al.: Genome-wide pleiotropy between Parkinson disease and autoimmune diseases. JAMA Neurol. 74, 780-792 (2017)