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Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly.
Uctepe E, Vona B, Esen FN, Sonmez FM, Smol T, Tümer S, Mancılar H, Geylan Durgun DE, Boute O, Moghbeli M, Ghayoor Karimiani E, Hashemi N, Bakhshoodeh B, Kim HG, Maroofian R, Yesilyurt A. Uctepe E, et al. Among authors: kim hg. Eur J Hum Genet. 2024 Jan;32(1):52-60. doi: 10.1038/s41431-023-01461-2. Epub 2023 Oct 26. Eur J Hum Genet. 2024. PMID: 37880421 Free PMC article.
Analysis of Cytogenetic Abnormalities in Iranian Patients with Syndromic Autism Spectrum Disorder: A Case Series.
Ghasemi MR, Zargari P, Sadeghi H, Bagheri S, Sadeghgi B, Mirfakhraie R, Ekrami M, Mohammadi Sarvaleh S, Hashemi Gorji F, Razjouyan K, Omrani D, Kim HG, Miryounesi M. Ghasemi MR, et al. Among authors: kim hg. Iran J Child Neurol. 2022 Spring;16(2):117-128. doi: 10.22037/ijcn.v16i4.34843. Epub 2022 Mar 14. Iran J Child Neurol. 2022. PMID: 35497098 Free PMC article.
Single Extracellular Vesicle Analysis Using Flow Cytometry for Neurological Disorder Biomarkers.
Ali Moussa HY, Manaph N, Ali G, Maacha S, Shin KC, Ltaief SM, Gupta V, Tong Y, Ponraj J, Salloum-Asfar S, Mansour S, Al-Shaban FA, Kim HG, Stanton LW, Grivel JC, Abdulla SA, Al-Shammari AR, Park Y. Ali Moussa HY, et al. Among authors: kim hg. Front Integr Neurosci. 2022 May 17;16:879832. doi: 10.3389/fnint.2022.879832. eCollection 2022. Front Integr Neurosci. 2022. PMID: 35655952 Free PMC article.
1,921 results