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Xinna Ji
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Xinna Ji
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Xinna Ji
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1
A de novo heterozygous variant in ACOX1 gene cause Mitchell syndrome: the first case in China and literature review
by
Mengxiao Shen
,
Qian Chen
,
Yanyan Gao
,
Hongyu Yan
,
Shuo Feng
,
Xinna Ji
,
Xue Zhang
Published 2023-07-01
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Article
2
Generation of a human iPSC line CIPi001-A from a benign familial infantile epilepsy patient related 16p11.2 deletion
by
Xinna Ji
,
Yanyan Gao
,
Pingping Zhang
,
Ziqi Jin
,
Yan Zhang
,
Minna Yang
,
Xue Zhang
,
Qian Chen
Published 2022-03-01
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Article
3
Generation of a human iPSC line CIPi003-A from a patient with focal epilepsy harboring a heterozygous mutation in DEPDC5 gene
by
Mengxiao Shen
,
Shiqi Fan
,
Fan Wu
,
Peidi Cheng
,
Yanyan Gao
,
Ping Zheng
,
Shuo Feng
,
Xinna Ji
,
Qian Chen
,
Xue Zhang
Published 2023-10-01
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Article
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