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Lanciotti, M., Indaco, S., Bonanomi, S., Coliva, T., Mastrodicasa, E., Caridi, G., et al. (2010). Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia. HAEMATOLOGICA, 95(1), 168-169 [10.3324/haematol.2009.015370].

Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia

COLIVA, TIZIANA ANGELA;
2010
Articolo in rivista - Articolo scientifico
Adaptor Proteins, Signal Transducing; Amino Acid Sequence; Child; Child, Preschool; Developmental Disabilities; Female; Humans; Italy; Male; Molecular Sequence Data; Mutation; Neutropenia; Pedigree; Severity of Illness Index; Hematology
English
2010
HAEMATOLOGICA
95
1
168
169
open
Lanciotti, M., Indaco, S., Bonanomi, S., Coliva, T., Mastrodicasa, E., Caridi, G., et al. (2010). Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia. HAEMATOLOGICA, 95(1), 168-169 [10.3324/haematol.2009.015370].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/67269
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