The ophthalmic diagnosis and management of four siblings with Werner syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://link.springer.com/content/pdf/10.1007/s10792-018-0929-8.pdf
Reference17 articles.
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2. Goto M (2008) Syndrome-causing mutations in Werner syndrome. Biosci Trends 2(4):147–150
3. Friedrich K, Lee L, Leistritz DF, Nürnberg G, Saha B, Hisama FM, Eyman DK, Lessel D, Nürnberg P, Li C, Garcia-F-Villalta MJ (2010) WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic–specific alterations. Hum Genet 128(1):103–111
4. Huang S, Lee L, Hanson NB, Lenaerts C, Hoehn H, Poot M, Rubin CD, Chen DF, Yang CC, Juch H, Dorn T (2006) The spectrum of WRN mutations in Werner syndrome patients. Hum Mutat 27(6):558–567
5. Rossi ML, Ghosh AK, Bohr VA (2010) Roles of Werner syndrome protein in protection of genome integrity. DNA Repair 9(3):331–344
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1. Optical coherence tomography findings in three patients with Werner syndrome;BMC Ophthalmology;2022-11-19
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