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A patient with Werner syndrome and adiponectin gene mutation

✍ Scribed by Naotake Hashimoto; Sachiko Hatanaka; Koutaro Yokote; Hiroko Kurosawa; Tomohiko Yoshida; Rie Iwai; Hidenori Takahashi; Katsuya Yoshida; Atsuya Horie; Kenichi Sakurai; Kazuo Yagui; Yasushi Saito; Shouji Yoshida


Book ID
118435506
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
250 KB
Volume
75
Category
Article
ISSN
0168-8227

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Werner syndrome and mutations of the WRN
✍ Nancy A. Uhrhammer; Laurence Lafarge; Laetitia Dos Santos; Anna Domaszewska; Mag πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 74 KB πŸ‘ 1 views

Werner syndrome (WS) is a pleiotropic disease of premature aging involving short stature, tight, atrophied, and/or ulcerated skin; a characteristic 'birdlike' facies and high, squeaky or hoarse voice; premature greying and thinning of the hair; and early onset cataracts. Additional common symptoms i