Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency

K. Matsubara, K. Imai, S. Okada, M. Miki, N. Ishikawa, M. Tsumura, T. Kato, O. Ohara, S. Nonoyama, M. Kobayashi
2007 Haematologica  
haematologica online 2007 haematologica/the hematology journal | 2007; 92(online) | e123 | K. Matsubara et al. | e124 | haematologica/the hematology journal | 2007; 92(online)
doi:10.3324/haematol.11973 pmid:18055975 fatcat:mwdg5pysqjdsxi27j3svfkzvdu