Publications

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Author Title [ Year(Desc)]
Filters: Author is Rosen, Aaron B I  [Clear All Filters]
2016
Petrovski, S. et al. Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures. Am J Hum Genet 98, 1001-1010 (2016).
2020
Chau, A. S. et al. Heme oxygenase-1 deficiency presenting with interstitial lung disease and hemophagocytic flares. Pediatr Rheumatol Online J 18, 80 (2020).
2021
Allenspach, E. J. et al. Germline SAMD9L truncation variants trigger global translational repression. J Exp Med 218, (2021).