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Year | Number of Results |
---|---|
2023 | 2 |
2024 | 2 |
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Page 1
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations.
Acta Neuropathol. 2024 Jan 9;147(1):13. doi: 10.1007/s00401-023-02665-y.
Acta Neuropathol. 2024.
PMID: 38194050
Free PMC article.
A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development.
Tsai MH, Lin WC, Chen SY, Hsieh MY, Nian FS, Cheng HY, Zhao HJ, Hung SS, Hsu CH, Hou PS, Tung CY, Lee MH, Tsai JW.
Tsai MH, et al.
Development. 2024 Jan 15;151(2):dev201912. doi: 10.1242/dev.201912. Epub 2024 Jan 18.
Development. 2024.
PMID: 38149472
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The Genetics of Primary Familial Brain Calcification: A Literature Review.
Chen SY, Ho CJ, Lu YT, Lin CH, Lan MY, Tsai MH.
Chen SY, et al.
Int J Mol Sci. 2023 Jun 29;24(13):10886. doi: 10.3390/ijms241310886.
Int J Mol Sci. 2023.
PMID: 37446066
Free PMC article.
Review.
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Long-Term Outcome of Neonatal Seizure with PACS2 Mutation: Case Series and Literature Review.
Chou IJ, Hou JY, Fan WL, Tsai MH, Lin KL.
Chou IJ, et al.
Children (Basel). 2023 Mar 26;10(4):621. doi: 10.3390/children10040621.
Children (Basel). 2023.
PMID: 37189870
Free PMC article.
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