Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency. (Q51970647)
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scientific article published in December 2007
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency. |
scientific article published in December 2007 |
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Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency. (English)
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Matsubara K
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Okada S
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Miki M
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Ishikawa N
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Tsumura M
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Kato T
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Nonoyama S
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Kobayashi M
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1 December 2007
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92
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12
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e123-5
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