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	<title>CiteULike: isami's Jackson</title>
	<description>CiteULike: isami's Jackson</description>


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    <title>Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation</title>
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    <description>&lt;i&gt;Brain, Vol. 130, No. 1. (January 2007), pp. 110-119.&lt;/i&gt;</description>
    <dc:title>Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation</dc:title>

    <dc:creator>Chinnery</dc:creator>
    <dc:creator>F Patrick</dc:creator>
    <dc:creator>Crompton</dc:creator>
    <dc:creator>E Douglas</dc:creator>
    <dc:creator>Birchall</dc:creator>
    <dc:creator>Daniel</dc:creator>
    <dc:creator>Jackson</dc:creator>
    <dc:creator>J Margaret</dc:creator>
    <dc:creator>Coulthard</dc:creator>
    <dc:creator>Alan</dc:creator>
    <dc:creator>Lombes</dc:creator>
    <dc:creator>Anne</dc:creator>
    <dc:creator>Quinn</dc:creator>
    <dc:creator>Niall</dc:creator>
    <dc:creator>Wills</dc:creator>
    <dc:creator>Adrian</dc:creator>
    <dc:creator>Fletcher</dc:creator>
    <dc:creator>Nicholas</dc:creator>
    <dc:creator>Mottershead</dc:creator>
    <dc:creator>P John</dc:creator>
    <dc:creator>Cooper</dc:creator>
    <dc:creator>Paul</dc:creator>
    <dc:creator>Kellett</dc:creator>
    <dc:creator>Mark</dc:creator>
    <dc:creator>Bates</dc:creator>
    <dc:creator>David</dc:creator>
    <dc:creator>Burn</dc:creator>
    <dc:creator>John</dc:creator>
    <dc:identifier>doi:10.1093/brain/awl319</dc:identifier>
    <dc:source>Brain, Vol. 130, No. 1. (January 2007), pp. 110-119.</dc:source>
    <dc:date>2006-12-22T14:33:47-00:00</dc:date>
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    <prism:startingPage>110</prism:startingPage>
    <prism:endingPage>119</prism:endingPage>
    <prism:publisher>Oxford University Press</prism:publisher>
    <prism:category>genomic</prism:category>
    <prism:category>neuroimaging</prism:category>
    <prism:category>parkinsonism</prism:category>
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