Identification and characterization of mutations in FANCL gene: A second case of Fanconi anemia belonging to FA-L complementation group-Reference-Cited by-同舟云学术

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Identification and characterization of mutations in FANCL gene: A second case of Fanconi anemia belonging to FA-L complementation group

Published:2009-07 Issue:7 Volume:30 Page:E761-E770
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Ali Abdullah Mahmood,Kirby Michelle,Jansen Michael,Lach Francis P.,Schulte Jennifer,Singh Thiyam Ramsing,Batish Sat D.,Auerbach Arleen D.,Williams David A.,Meetei Amom Ruhikanta

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 23 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. E3 ligases: a ubiquitous link between DNA repair, DNA replication and human disease;Biochemical Journal;2024-07-10

2. Exploring the hub genes and potential drugs involved in Fanconi anemia using microarray datasets and bioinformatics analysis;Journal of Biomolecular Structure and Dynamics;2023-12-27

3. An acquired BMF with FANCL gene heterozygous mutation: Case report;Medicine;2023-06-16

4. Pan-cancer analysis of the prognostic and immunological role of Fanconi anemia complementation group E;Frontiers in Genetics;2023-01-04

5. FANCL supports Parkin-mediated mitophagy in a ubiquitin ligase-independent manner;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2022-09

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