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Paper Details

A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51.
Nat Commun
110
2015
DNA repair gene, DNA repair gene RAD51, FA, FA-, Fanconi anaemia, RAD51, allele, bone marrow failure, cancer, congenital mirror movement disorders, developmental abnormalities, g, hereditary disease, hypersensitivity, mental retardation, microcephaly, p.Ala293Thr, paediatric cancers, patient
Author NameAffiliation
Gustavo GlusmanInstitute for Systems Biology
Jared C RoachInstitute for Systems Biology
Leroy HoodInstitute for Systems Biology
Leroy HoodInstitute for Systems Biology
Johan T den DunnenDepartment of Human and Clinical Genetics, Leiden University Medical Center
Josephine C DorsmanVU University Medical Center
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Release 1.2