Whole‐Exome Sequencing Identified Rare Variants in PCDHGB1 in Patients with Adult‐Onset Dystonia

Whole‐Exome Sequencing Identified Rare Variants in PCDHGB1 in Patients with Adult‐Onset Dystonia
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DOI:
10.1002/mds.28965
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发表时间:
2022
期刊:
Movement Disorders
影响因子:
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通讯作者:
Ling‐Jing Jin
Ling‐Jing Jin
中科院分区:
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文献类型:
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作者:
Li‐Xi Li;Jie‐Hong Huang;Li‐Zhen Pan;Xiao‐Long Zhang;You‐Gui Pan;Ling‐Jing Jin

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