Progressive multifocal leukoencephalopathy in a patient with novel mutation in the RAC2 gene: a case report.

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Title: Progressive multifocal leukoencephalopathy in a patient with novel mutation in the RAC2 gene: a case report.
Authors: Bahrami, Sima1 (AUTHOR), Arshi, Saba1 (AUTHOR), Nabavi, Mohammad1 (AUTHOR), Bemanian, Mohammad Hassan1 (AUTHOR), Fallahpour, Morteza1 (AUTHOR), Rezaeifar, Afshin1 (AUTHOR), Shokri, Sima1 (AUTHOR) Shokri.s@iums.ac.ir
Source: Journal of Medical Case Reports. 6/11/2022, Vol. 16 Issue 1, p1-5. 5p.
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  Data: Progressive multifocal leukoencephalopathy in a patient with novel mutation in the RAC2 gene: a case report.
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  Data: <searchLink fieldCode="AR" term="%22Bahrami%2C+Sima%22">Bahrami, Sima</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Arshi%2C+Saba%22">Arshi, Saba</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Nabavi%2C+Mohammad%22">Nabavi, Mohammad</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bemanian%2C+Mohammad+Hassan%22">Bemanian, Mohammad Hassan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fallahpour%2C+Morteza%22">Fallahpour, Morteza</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Rezaeifar%2C+Afshin%22">Rezaeifar, Afshin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Shokri%2C+Sima%22">Shokri, Sima</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> Shokri.s@iums.ac.ir</i>
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Medical+Case+Reports%22">Journal of Medical Case Reports</searchLink>. 6/11/2022, Vol. 16 Issue 1, p1-5. 5p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=158205490
RecordInfo BibRecord:
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    Identifiers:
      – Type: doi
        Value: 10.1186/s13256-022-03333-7
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      – Code: eng
        Text: English
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      – TitleFull: Progressive multifocal leukoencephalopathy in a patient with novel mutation in the RAC2 gene: a case report.
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            NameFull: Bahrami, Sima
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            NameFull: Arshi, Saba
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            NameFull: Nabavi, Mohammad
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            NameFull: Bemanian, Mohammad Hassan
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            NameFull: Fallahpour, Morteza
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            NameFull: Rezaeifar, Afshin
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            NameFull: Shokri, Sima
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            – D: 11
              M: 06
              Text: 6/11/2022
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              Y: 2022
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            – TitleFull: Journal of Medical Case Reports
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