Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia-Reference-Cited by-同舟云学术

Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia

Published:2008-08 Issue:8 Volume:128 Page:2055-2068
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Inui Hiroki,Oh Kyu-Seon,Nadem Carine,Ueda Takahiro,Khan Sikandar G.,Metin Ahmet,Gozukara Engin,Emmert Steffen,Slor Hanoch,Busch David B.,Baker Carl C.,DiGiovanna John J.,Tamura Deborah,Seitz Cornelia S.,Gratchev Alexei,Wu Wen Hao,Chung Kee Yang,Chung Hye Jin,Azizi Esther,Woodgate Roger,Schneider Thomas D.,Kraemer Kenneth H.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference77 articles.

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1. Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant;Scientific Reports;2024-01-11

2. Deep intronic founder mutations identified in the ERCC4 / XPF gene are potential therapeutic targets for a high-frequency form of xeroderma pigmentosum;Proceedings of the National Academy of Sciences;2023-06-26

3. Current state of knowledge of human DNA polymerase eta protein structure and disease-causing mutations;Mutation Research/Reviews in Mutation Research;2022-07

4. Current state of knowledge of human DNA polymerase eta protein structure and disease-causing mutations;MUTAT RES-REV MUTAT;2022

5. Variant subtype of xeroderma pigmentosum diagnosed in a 63-year-old woman;European Journal of Dermatology;2022-07-01