Browsing Centre for Genomics and Child Health by Author "Luzzatto, L"
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Germline NPM1 mutations lead to altered rRNA 2 '-O-methylation and cause dyskeratosis congenita
Nachmani, D; Bothmer, AH; Grisendi, S; Mele, A; Bothmer, D; Lee, JD; Monteleone, E; Cheng, K; Zhang, Y; Bester, AC (2019-10) -
New WHO classification of genetic variants causing G6PD deficiency.
Luzzatto, L; Bancone, G; Dugué, P-A; Jiang, W; Minucci, A; Nannelli, C; Pfeffer, D; Prchal, J; Sirdah, M; Sodeinde, O (2024-08-01)