Two novel variants of the STXBP1 and CHRNB2 genes identified in a Chinese boy with refractory seizures and developmental delay

aDepartment of Neurology and Development, Senior Department of Pediatrics, the Seventh Medical Center of PLA General Hospital

bDepartment of Neurology and Development, National Engineering Laboratory for Birth Defects Prevention and Control of Key Technology

cDepartment of Neurology and Development, Beijing Key Laboratory of Pediatric Organ Failure

dBeijing GrandOmics Biosciences Co., Ltd, Beijing, China

Received 9 March 2023 Accepted 8 May 2023.

*Sanmei Wang and Di Cui contributed equally to the writing of this article.

Supplemental Digital Content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal's website, www.psychgenetics.com.

Correspondence to Sanmei Wang, MD, Department of Neurology and Development, Senior Department of Pediatrics, the Seventh Medical Center of PLA General Hospital, 5 Nan Men Cang Hu Tong, Dongcheng District, Beijing 100700, China, Tel: +86 13683383295; fax: 010 66721838; e-mail: [email protected]

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