Neurodegenerative disorder with brain iron accumulation previously known as SENDA syndrome now genetically determined.
Identifieur interne : 000894 ( Main/Exploration ); précédent : 000893; suivant : 000895Neurodegenerative disorder with brain iron accumulation previously known as SENDA syndrome now genetically determined.
Auteurs : Petr Dusek [République tchèque] ; Susanne A. SchneiderSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Carrier Proteins.
- genetics : Iron Overload.
- metabolism : Brain.
- Exome, Female, Genes, X-Linked, Humans, Male, Mutation, Phenotype.
DOI: 10.1002/mds.25424
PubMed: 23868373
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000825
- to stream PubMed, to step Curation: 000825
- to stream PubMed, to step Checkpoint: 000909
- to stream Ncbi, to step Merge: 003C57
- to stream Ncbi, to step Curation: 003C57
- to stream Ncbi, to step Checkpoint: 003C57
- to stream Main, to step Merge: 000894
- to stream Main, to step Curation: 000894
Le document en format XML
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<author><name sortKey="Dusek, Petr" sort="Dusek, Petr" uniqKey="Dusek P" first="Petr" last="Dusek">Petr Dusek</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Neurology, Center of Clinical Neuroscience, 1st Faculty of Medicine General University Hospital in Prague, Charles University in Prague, Prague, Czech Republic.</nlm:affiliation>
<country xml:lang="fr">République tchèque</country>
<wicri:regionArea>Department of Neurology, Center of Clinical Neuroscience, 1st Faculty of Medicine General University Hospital in Prague, Charles University in Prague, Prague</wicri:regionArea>
<placeName><settlement type="city">Prague</settlement>
<region type="région" nuts="2">Bohême centrale</region>
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<author><name sortKey="Schneider, Susanne A" sort="Schneider, Susanne A" uniqKey="Schneider S" first="Susanne A" last="Schneider">Susanne A. Schneider</name>
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<affiliation wicri:level="3"><nlm:affiliation>Department of Neurology, Center of Clinical Neuroscience, 1st Faculty of Medicine General University Hospital in Prague, Charles University in Prague, Prague, Czech Republic.</nlm:affiliation>
<country xml:lang="fr">République tchèque</country>
<wicri:regionArea>Department of Neurology, Center of Clinical Neuroscience, 1st Faculty of Medicine General University Hospital in Prague, Charles University in Prague, Prague</wicri:regionArea>
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<author><name sortKey="Schneider, Susanne A" sort="Schneider, Susanne A" uniqKey="Schneider S" first="Susanne A" last="Schneider">Susanne A. Schneider</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
<imprint><date when="2013" type="published">2013</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Brain (metabolism)</term>
<term>Carrier Proteins (genetics)</term>
<term>Exome</term>
<term>Female</term>
<term>Genes, X-Linked</term>
<term>Humans</term>
<term>Iron Overload (genetics)</term>
<term>Male</term>
<term>Mutation</term>
<term>Phenotype</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Carrier Proteins</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Iron Overload</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Brain</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Exome</term>
<term>Female</term>
<term>Genes, X-Linked</term>
<term>Humans</term>
<term>Male</term>
<term>Mutation</term>
<term>Phenotype</term>
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<tree><noCountry><name sortKey="Schneider, Susanne A" sort="Schneider, Susanne A" uniqKey="Schneider S" first="Susanne A" last="Schneider">Susanne A. Schneider</name>
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