Varaico: Literature-Extracted Genetic Variants

Gene:WRN
Variant:p.H558fs
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WRN

NM_000553.6:p.H558fs

Associated Papers

A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome.

Wu PF et al.

Molecular Medicine Reports, 2017

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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."