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Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.
Moniz, H; Gastou, M; Leblanc, T; Hurtaud, C; Crétien, A; Lécluse, Y; Raslova, H; Larghero, J; Croisille, L; Faubladier, M; Bluteau, O; Lordier, L; Tchernia, G; Vainchenker, W; Mohandas, N; Da Costa, L.
Affiliation
  • Moniz H; INSERM UMR U1009, Institut Gustave Roussy, Villejuif, France.
Cell Death Dis ; 3: e356, 2012 Jul 26.
Article in En | MEDLINE | ID: mdl-22833095

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ribosomal Proteins / Anemia, Diamond-Blackfan / Erythroid Cells Limits: Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Cell Death Dis Year: 2012 Document type: Article Affiliation country: Francia Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ribosomal Proteins / Anemia, Diamond-Blackfan / Erythroid Cells Limits: Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Cell Death Dis Year: 2012 Document type: Article Affiliation country: Francia Country of publication: Reino Unido