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Genetic genealogy uncovers a founder deletion mutation in the cerebral cavernous malformations 2 gene.
Hum Genet. 2022 Nov;141(11):1761-1769. doi: 10.1007/s00439-022-02458-5. Epub 2022 Apr 30.
Hum Genet. 2022.
PMID: 35488064
Free PMC article.
COVID-19 in a Hemorrhagic Neurovascular Disease, Cerebral Cavernous Malformation.
Shkoukani A, Srinath A, Stadnik A, Girard R, Shenkar R, Sheline A, Dahlem K, Lee C, Flemming K, Awad IA.
Shkoukani A, et al. Among authors: sheline a.
J Stroke Cerebrovasc Dis. 2021 Nov;30(11):106101. doi: 10.1016/j.jstrokecerebrovasdis.2021.106101. Epub 2021 Sep 8.
J Stroke Cerebrovasc Dis. 2021.
PMID: 34520969
Free PMC article.
No abstract available.
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Somatic SLC35A2 mosaicism correlates with clinical findings in epilepsy brain tissue.
Miller KE, Koboldt DC, Schieffer KM, Bedrosian TA, Crist E, Sheline A, Leraas K, Magrini V, Zhong H, Brennan P, Bush J, Fitch J, Bir N, Miller AR, Cottrell CE, Leonard J, Pindrik JA, Rusin JA, Shah SH, White P, Wilson RK, Mardis ER, Pierson CR, Ostendorf AP.
Miller KE, et al. Among authors: sheline a.
Neurol Genet. 2020 Jun 17;6(4):e460. doi: 10.1212/NXG.0000000000000460. eCollection 2020 Aug.
Neurol Genet. 2020.
PMID: 32637635
Free PMC article.
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