Publications by authors named "Jonathan F Wing"

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A Distinct Genotype of XP Complementation Group A: Surprisingly Mild Phenotype Highly Prevalent in Northern India/Pakistan/Afghanistan.
Mieran Sethi, Shaheen Haque, Heather Fawcett, Jonathan F Wing, Natalie Chandler

J Invest Dermatol· April 2016

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Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.
Kazuya Kashiyama, Yuka Nakazawa, Daniela T Pilz, Chaowan Guo, Mayuko Shimada, Jonathan F Wing

Am J Hum Genet· May 2013

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Neurological symptoms and natural course of xeroderma pigmentosum.
Anu Anttinen, Leena Koulu, Eeva Nikoskelainen, Raija Portin, Timo Kurki, Jonathan F Wing

Brain· August 2008

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Translesion synthesis: Y-family polymerases and the polymerase switch.
Alan R Lehmann, Atsuko Niimi, Tomoo Ogi, Stephanie Brown, Simone Sabbioneda, Jonathan F Wing

DNA Repair (Amst)· July 2007

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