A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype.
Schultz-Rogers L, Lach FP, Rickman KA, Ferrer A, Mangaonkar AA, Schwab TL, Schmitz CT, Clark KJ, Dsouza NR, Zimmermann MT, Litzow M, Jacobi N, Klee EW, Smogorzewska A, Patnaik MM.
Schultz-Rogers L, et al. Among authors: patnaik mm.
Haematologica. 2021 Apr 1;106(4):1188-1192. doi: 10.3324/haematol.2020.259275.
Haematologica. 2021.
PMID: 32646888
Free PMC article.
No abstract available.