The spectrum ofWRNmutations in Werner syndrome patients

Huang, Shurong; Lee, Lin; Hanson, Nancy; Lenaerts, C; Hoehn, Holger; Poot, Martin; D. Rubin, Craig; Chen, Da-Fu; Yang, Chih‐Chao; Juch, Heike; Dorn, Thomas; Spiegel, Roland; A Oral, Elif; Abid, Mohammed; Battisti, Carla; Lucci‐Cordisco, Emanuela; Neri, Giovanni; H. Steed, Erin; Kidd, Alexa; L. Isley, William; Showalter, David; L. Vittone, Janet; Konstantinow, A.; Ring, Johannes; Meyer, Peter; L. Wenger, Sharon; von Herbay, A.; Wollina, Uwe; Schuelke, Markus; R. Huizenga, Carin; F. Leistritz, Dru; M. Martin, George; I. Mian, Shahzad; Oshima, Junko

doi:10.1002/humu.20337

Public

The spectrum ofWRNmutations in Werner syndrome patients

Published in Human Mutation • May 3, 2006

Authors:

Shurong Huang

Lin Lee

Nancy Hanson

Abstract

The International Registry of Werner syndrome (www.wernersyndrome.org) has been providing molecular diagnosis of the Werner syndrome (WS) for the past decade. The present communication summarizes, from among 99 WS subjects, the spectrum of 50 distinct mutations discovered by our group and by others ...

Subject

Biology

Werner syndrome

Genetics

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