Founder Haplotype Analysis of Fanconi Anemia in the Korean Population Finds Common Ancestral Haplotypes for aFANCGVariant-Reference-Cited by-同舟云学术

Founder Haplotype Analysis of Fanconi Anemia in the Korean Population Finds Common Ancestral Haplotypes for aFANCGVariant

Published:2015-02-20 Issue:3 Volume:79 Page:153-161
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Park Joonhong¹²,Kim Myungshin¹²,Jang Woori¹²,Chae Hyojin¹²,Kim Yonggoo¹²,Chung Nack-Gyun³,Lee Jae-Wook³,Cho Bin³,Jeong Dae-Chul³,Park In Yang⁴,Park Mi Sun⁵

Affiliation:

1. Department of Laboratory Medicine, College of Medicine; The Catholic University of Korea; Seoul Republic of Korea

2. Catholic Genetic Laboratory Center, College of Medicine; The Catholic University of Korea; Seoul Republic of Korea

3. Department of Pediatrics, College of Medicine; The Catholic University of Korea; Seoul Republic of Korea

4. Department of Obstetrics and Gynecology, College of Medicine; The Catholic University of Korea; Seoul Republic of Korea

5. Department of Biostatistics, Clinical Research Coordinating Center; The Catholic University of Korea; Seoul Republic of Korea

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ahg.12097/fullpdf

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3. Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia;Bogliolo;Am J Hum Genet,2013

4. A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain;Callen;Blood,2005

5. Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations;Castella;Blood,2011

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2. Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG;International Journal of Molecular Sciences;2022-02-20

3. Spectrum of Germline Mutations Within Fanconi Anemia–Associated Genes Across Populations of Varying Ancestry;JNCI Cancer Spectrum;2021-01-05

4. Screening for mutations in two exons of FANCG gene in Pakistani population;Biomedical Papers;2017-06-14