TG c.668_669insAGGA ;(p.F224Gfs*8)

Variant ID: 8-133894137-C-CAGGA

NM_003235.4(TG):c.668_669insAGGA;(p.F224Gfs*8)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Molecular Diagnosis of Panel-Based Next-Generation Sequencing Approach and Clinical Symptoms in Patients With Glycogen Storage Disease: A Single Center Retrospective Study.

Frontiers In Pediatrics
Ying, Shen S; Zhihua, Zhang Z; Yucan, Zheng Z; Yu, Jin J; Qian, Lin L; Bixia, Zheng Z; Weixia, Cheng C; Zhifeng, Liu L
Publication Date: 2020

Variant appearance in text: TG: 668_669insAGGA
PubMed Link: 33344388
Variant Present in the following documents:
  • Main text
  • fped-08-600446.pdf
View BVdb publication page