A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype
- Resource Type
- article
- Source
- Haematologica, Vol 106, Iss 4 (2020)
- Subject
Diseases of the blood and blood-forming organs RC633-647.5 - Language
- English
- ISSN
- 0390-6078
1592-8721