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STUB1-Associated Autosomal-Recessive Spinocerebellar Ataxia Type 16 (SCAR16) Presenting with Gordon-Holmes Syndrome Caused by Maternal Uniparental Isodisomy.
Agianda HAP, Tam A, Kunta A, Zubair U, Saffari A, Rong J, Crough M, Srouji R, Quiroz V, Yang K, Schierbaum L, Ebrahimi-Fakhari D. Agianda HAP, et al. Among authors: kunta a. Mov Disord Clin Pract. 2024 Dec 27. doi: 10.1002/mdc3.14322. Online ahead of print. Mov Disord Clin Pract. 2024. PMID: 39728009 No abstract available.
Sex differences in brain transcriptomes of juvenile Cynomolgus macaques.
Kabbej N, Ashby FJ, Riva A, Gamlin PD, Mande RJ, Kunta A, Rouse CJ, Heldermon CD. Kabbej N, et al. Among authors: kunta a. Res Sq [Preprint]. 2023 Nov 20:rs.3.rs-3422091. doi: 10.21203/rs.3.rs-3422091/v1. Res Sq. 2023. PMID: 38045237 Free PMC article. Preprint.
Disease correction in mucopolysaccharidosis type IIIB mice by intraparenchymal or cisternal delivery of a capsid modified AAV8 codon-optimized NAGLU vector.
Rouse CJ, Hawkins K, Kabbej N, Dalugdug J, Kunta A, Kim MJ, Someya S, Herbst Z, Gelb M, Dinelli I, Butterworth E, Falk DJ, Rosenkrantz E, Elmohd H, Khaledi H, Mowafy S, Ashby F, Heldermon CD. Rouse CJ, et al. Among authors: kunta a. Hum Mol Genet. 2023 Jan 13;32(3):417-430. doi: 10.1093/hmg/ddac209. Hum Mol Genet. 2023. PMID: 35997776 Free PMC article.
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