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Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene

✍ Scribed by Ishikawa, N; Okada, S; Miki, M; Shirao, K; Kihara, H; Tsumura, M; Nakamura, K; Kawaguchi, H; Ohtsubo, M; Yasunaga, S; Matsubara, K; Sako, M; Hara, J; Shiohara, M; Kojima, S; Sato, T; Takihara, Y; Kobayashi, M

Book ID: 127286661
Publisher: BMJ Publishing Group
Year: 2008
Tongue: English
Weight: 569 KB
Volume: 45
Category: Article
ISSN: 0022-2593
DOI: 10.1136/jmg.2008.058297

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