Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency.
- DOI
- 10.3324/haematol.11973
- Published
- 2007 Dec
- Container
- Haematologica
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.3324/haematol.11973,
title = {Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency.},
author = {Matsubara K and Imai K and Okada S and Miki M and Ishikawa N and Tsumura M and Kato T and Ohara O and Nonoyama S and Kobayashi M},
year = {2007},
journal = {Haematologica},
doi = {10.3324/haematol.11973},
url = {https://doi.org/10.3324/haematol.11973}
}RIS
TY - JOUR TI - Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency. AU - Matsubara K AU - Imai K AU - Okada S AU - Miki M AU - Ishikawa N AU - Tsumura M AU - Kato T AU - Ohara O AU - Nonoyama S AU - Kobayashi M PY - 2007 JO - Haematologica DO - 10.3324/haematol.11973 UR - https://doi.org/10.3324/haematol.11973 ER -
APA
K, M., K, I., S, O., M, M., N, I., M, T., T, K., O, O., S, N., & M, K. (2007). Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency.. Haematologica. https://doi.org/10.3324/haematol.11973
Source records
- pubmed · retrieved 2026-11-10T11:12:06.888Z