Werner syndrome and mutations of the WRN and LMNA genes in France
Werner syndrome and mutations of the WRN and LMNA genes in France
About this item
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Author / Creator
Publisher
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title
Language
English
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Publication information
Publisher
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Subjects
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Scope and Contents
Contents
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 include diabetes mellitus, hypogonadism, osteoporos...
Alternative Titles
Full title
Werner syndrome and mutations of the WRN and LMNA genes in France
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Record Identifier
TN_cdi_proquest_miscellaneous_68573182
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_68573182
Other Identifiers
ISSN
1059-7794
E-ISSN
1098-1004
DOI
10.1002/humu.9435
