TSC2 c.2837+2T>C

Variant ID: 16-2126588-T-C

NM_000548.3(TSC2):c.2837+2T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


[Gene mutations in unexplained infantile epileptic encephalopathy: an analysis of 47 cases].

Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal Of Contemporary Pediatrics
Wei, Chun-Miao CM; Xia, Gui-Zhi GZ; Ren, Rong-Na RN
Publication Date: 2018-02

Variant appearance in text: TSC2: 2837+2T>C
PubMed Link: 29429461
Variant Present in the following documents:
  • Main text
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