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Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.

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Title: Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.
Authors: Jiao, Jun-Ping1,2 (AUTHOR), Zhang, Hong-Wei3 (AUTHOR), Zhou, Xi-Zhong4 (AUTHOR), Tian, Shu-Juan2 (AUTHOR), Gao, Li5 (AUTHOR), Li, Bing-Mei1 (AUTHOR), Luo, Jun-Xia3 (AUTHOR), Wang, Jie1 (AUTHOR), Lan, Song6 (AUTHOR) 1355345327@qq.com, Li, Bin1 (AUTHOR) lcmlibin@163.com, Liao, Wei-Ping1 (AUTHOR)
Source: Orphanet Journal of Rare Diseases. 7/28/2025, Vol. 20 Issue 1, p1-11. 11p.
Database: Academic Search Ultimate
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  Data: Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.
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  Data: <searchLink fieldCode="AR" term="%22Jiao%2C+Jun-Ping%22">Jiao, Jun-Ping</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Hong-Wei%22">Zhang, Hong-Wei</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhou%2C+Xi-Zhong%22">Zhou, Xi-Zhong</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Tian%2C+Shu-Juan%22">Tian, Shu-Juan</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gao%2C+Li%22">Gao, Li</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Bing-Mei%22">Li, Bing-Mei</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Luo%2C+Jun-Xia%22">Luo, Jun-Xia</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Jie%22">Wang, Jie</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lan%2C+Song%22">Lan, Song</searchLink><relatesTo>6</relatesTo> (AUTHOR)<i> 1355345327@qq.com</i><br /><searchLink fieldCode="AR" term="%22Li%2C+Bin%22">Li, Bin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> lcmlibin@163.com</i><br /><searchLink fieldCode="AR" term="%22Liao%2C+Wei-Ping%22">Liao, Wei-Ping</searchLink><relatesTo>1</relatesTo> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 7/28/2025, Vol. 20 Issue 1, p1-11. 11p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186951834
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        Value: 10.1186/s13023-025-03924-9
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      – TitleFull: Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.
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              M: 07
              Text: 7/28/2025
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              Y: 2025
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