Varaico: Literature-Extracted Genetic Variants

Gene:STXBP1
Variant:p.E221_G222Splc
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STXBP1

NM_001032221.6:p.E221_G222Splc

Associated Papers

Case report: A novel STXBP1 splice variant and the landscape of splicing-involved STXBP1-related disorders.

Wang H et al.

Frontiers in Neurology, 2023

37056358 (PubMed )
Supplement: Table_1.XLSX › 54_canonical

Clinical and molecular characteristics of 69 Chinese patients with ornithine transcarbamylase deficiency.

Lu D et al.

Orphanet Journal of Rare Diseases, 2020

[Clinical characteristics and analysis of mass spectrometric data in patients with ornithine transcarbamylase deficiency].

Han F et al.

Zhonghua Yi Xue Za Zhi, 2014

[Comparison and clinical application of two methods for determination of plasma chitotriosidase activity].

Wang Y et al.

Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2012

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."