Phenotypic and genotypic correlation evaluation of 148 pediatric patients with Fanconi anemia in a Chinese rare disease cohort-Reference-Cited by-同舟云学术

Phenotypic and genotypic correlation evaluation of 148 pediatric patients with Fanconi anemia in a Chinese rare disease cohort

Published:2023-01 Issue: Volume:539 Page:41-49
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Chang Lixian,Zhang Li,An Wenbin,Wan Yang,Cai Yuli,Lan Yang,Zhang Aoli,Liu Lipeng,Ruan Min,Liu Xiaoming,Guo Ye,Yang Wenyu,Chen Xiaojuan,Chen Yumei,Wang Shuchun,Zou Yao,Yuan Weiping,Zhu Xiaofan

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference38 articles.

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2. Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia;Mamrak;Blood Rev.,2017

3. RFWD3-Mediated Ubiquitination Promotes Timely Removal of Both RPA and RAD51 from DNA Damage Sites to Facilitate Homologous Recombination;Inano;Mol Cell.,2017

4. FANCD2 and DNA Damage;Nepal;Int J Mol Sci.,2017

5. Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia;Knies;J Clin Invest.,2017

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