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[New types of microcytic anemia].
Iolascon A, De Falco L, Boschetto L, Piscopo C, Pirolo C, Di Noce F. Iolascon A, et al. Among authors: de falco l. Minerva Pediatr. 2007 Oct;59(5):525-7. Minerva Pediatr. 2007. PMID: 17947902 Italian. No abstract available.
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.
Schwarz K, Iolascon A, Verissimo F, Trede NS, Horsley W, Chen W, Paw BH, Hopfner KP, Holzmann K, Russo R, Esposito MR, Spano D, De Falco L, Heinrich K, Joggerst B, Rojewski MT, Perrotta S, Denecke J, Pannicke U, Delaunay J, Pepperkok R, Heimpel H. Schwarz K, et al. Among authors: de falco l. Nat Genet. 2009 Aug;41(8):936-40. doi: 10.1038/ng.405. Epub 2009 Jun 28. Nat Genet. 2009. PMID: 19561605 Free article.
Beta-spectrinBari: a truncated beta-chain responsible for dominant hereditary spherocytosis.
Perrotta S, Della Ragione F, Rossi F, Avvisati RA, Di Pinto D, De Mieri G, Scianguetta S, Mancusi S, De Falco L, Marano V, Iolascon A. Perrotta S, et al. Among authors: de mieri g, de falco l. Haematologica. 2009 Dec;94(12):1753-7. doi: 10.3324/haematol.2009.010124. Epub 2009 Jul 16. Haematologica. 2009. PMID: 19608679 Free PMC article.
67 results