Whole-exome sequencing of Fanconi anemia
We performed whole-exome sequencing of two Fanconi anemia patients without mutation of known FA genes, and identified a novel FA gene FANCT.
- Type: Other
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
Dataset ID | Description | Technology | Samples |
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EGAD00001001302 | Illumina HiSeq 2500 | 2 |
Publications | Citations |
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Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia.
Am J Hum Genet 96: 2015 1001-1007 |
79 |