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. Author manuscript; available in PMC: 2014 Apr 1.
Published in final edited form as: Mutat Res. 2012 Dec 28;752(2):138–152. doi: 10.1016/j.mrrev.2012.12.004

Figure 5. Clinically relevant missense mutations in WRN helicase-nuclease responsible for Werner syndrome.

Figure 5

See text for details. For a comprehensive listing of WRN mutations, see The International Registry of Werner Syndrome www.wernersyndrome.org; also see [91]. The high affinity RPA70 interaction domain of WRN [139] is indicated. WRN exonuclease domain (EXO) and NLS are also shown. See text for details.