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- W2559589619 abstract "FA is a rare recessive genetic disorder with autosomal or X-linked mode of inheritance and is associated with 19 different FA complementation groups. We have studied three patients clinically diagnosed as FA. All three patients showed a high frequency chromosomal breakage in MMC induced blood cultures and FANCD2 non-monoubiquitination by western blotting. The molecular analysis using direct sequencing revealed two novel mutations in FANCG; 2 novel mutations c.1143+5G>C and c.883dupG, and a reported mutation c.1471_1473delAAAinsG. We have for the first time modeled FANCG protein with fold based template search using pGenthreader which revealed sequence fold identical to super helical TPR domain of O linked GLCNAC transferase and have studied the impact of mutations on the function and structure of FANCG. All three mutations are potential pathogenic molecular changes which can affect FANCG interactions required for FA pathway, homologous recombination repairs and unhooking step of the ICL repair process." @default.
- W2559589619 created "2016-12-08" @default.
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- W2559589619 date "2017-02-01" @default.
- W2559589619 modified "2023-09-24" @default.
- W2559589619 title "Characterization of two novel FANCG mutations in Indian Fanconi anemia patients" @default.
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- W2559589619 doi "https://doi.org/10.1016/j.leukres.2016.11.013" @default.
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