Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds (Q46226931)
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scientific article published on 22 November 2008
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English | Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds |
scientific article published on 22 November 2008 |
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Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds (English)
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David C Linch
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Rosemary E Gale
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Bradley N Smith
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Phil J Ancliff
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Asim Khwaja
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22 November 2008
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144
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5
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762-770
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Identifiers
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