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            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>Coronavirus</text>
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            <name>Description</name>
            <description>An account of the resource</description>
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                <text>Dominio científico: Coronavirus</text>
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      <name>Dublin Core</name>
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        <element elementId="50">
          <name>Title</name>
          <description>A name given to the resource</description>
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              <text>Lack of association between polymorphisms of &lt;it&gt;MASP2 &lt;/it&gt;and susceptibility to SARS coronavirus infection</text>
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          <name>Creator</name>
          <description>An entity primarily responsible for making the resource</description>
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            <elementText elementTextId="22640">
              <text>Yang Ruifu, Ma Qingjun, Liu Chuanxuan, Li Ping, Shi Yuling, Yan Jiangwei, Wang Yan, Wang Xiaoyi, zhu Lina, Yang Xiao, Cao Cheng</text>
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          <name>Description</name>
          <description>An account of the resource</description>
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              <text>Abstract Background The pathogenesis of severe acute respiratory disease syndrome (SARS) is not fully understood. One case-control study has reported an association between susceptibility to SARS and mannan-binding lectin (MBL) in China. As the downstream protein of MBL, variants of the MBL-associated serine protease-2 (MASP2) gene may be associated with SARS coronavirus (SARS-CoV) infection in the same population. Methods Thirty individuals with SARS were chosen for analysis of MASP2 polymorphisms by means of PCR direct sequencing. Tag single nucleotide polymorphisms (tagSNPs) were chosen using pairwise tagging algorithms. The frequencies of four tag SNPs (rs12711521, rs2261695, rs2273346 and rs7548659) were ascertained in 376 SARS patients and 523 control subjects, using the Beckman SNPstream Ultra High Throughput genotyping platform. Results There is no significant association between alleles or genotypes of the MASP2 tagSNP and susceptibility to SARS-CoV in both Beijing and Guangzhou populations. Diplotype (rs2273346 and rs12711521)were analyzed for association with susceptibility to SARS, no statistically significant evidence of association was observed. The Beijing and Guangzhou sample groups were homogeneous regarding demographic and genetic parameters, a joined analysis also showed no statistically significant evidence of association. Conclusion Our data do not suggest a role for MASP2 polymorphisms in SARS susceptibility in northern and southern China.</text>
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          <name>Date</name>
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              <text>2009</text>
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          <name>Identifier</name>
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              <text>DOI: 10.1186/1471-2334-9-51</text>
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          <name>Source</name>
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              <text>BMC Infectious Diseases</text>
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          <name>Publisher</name>
          <description>An entity responsible for making the resource available</description>
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            <elementText elementTextId="22645">
              <text>BMC</text>
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          <name>Coverage</name>
          <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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            <elementText elementTextId="22646">
              <text>Infectious and parasitic diseases</text>
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          <name>Language</name>
          <description>A language of the resource</description>
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              <text>EN</text>
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