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A further family of Stromme syndrome carrying CENPF mutation.
Ozkinay F, Atik T, Isik E, Gormez Z, Sagiroglu M, Sahin OA, Corduk N, Onay H. Ozkinay F, et al. Am J Med Genet A. 2017 Jun;173(6):1668-1672. doi: 10.1002/ajmg.a.38173. Epub 2017 Apr 13. Am J Med Genet A. 2017. PMID: 28407396
Treatment of Depression in Huntington's Disease: A Systematic Review.
Zadegan SA, Ramirez F, Reddy KS, Sahin O, Rocha NP, Teixeira AL, Furr Stimming E. Zadegan SA, et al. Among authors: sahin o. J Neuropsychiatry Clin Neurosci. 2024 Mar 26:appineuropsych20230120. doi: 10.1176/appi.neuropsych.20230120. Online ahead of print. J Neuropsychiatry Clin Neurosci. 2024. PMID: 38528808
807 results