MovDisordV3, Main, Exploration, bibRecord, 000160

Mutations in HTRA2 are not a common cause of familial classic ET.

Identifieur interne : 000160 ( Main/Exploration ); précédent : 000159; suivant : 000161

Mutations in HTRA2 are not a common cause of familial classic ET.

Auteurs : Franziska Hopfner [Allemagne] ; Stefanie H. Müller [Allemagne] ; Delia Lorenz [Allemagne] ; Silke Appenzeller [Allemagne] ; Stephan Klebe [Allemagne] ; Günther Deuschl [Allemagne] ; Gregor Kuhlenb Umer [Allemagne]

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.

RBID : pubmed:25970799
DOI: 10.1002/mds.26252
PubMed: 25970799

Affiliations:

Le document en format XML

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<author><name sortKey="Hopfner, Franziska" sort="Hopfner, Franziska" uniqKey="Hopfner F" first="Franziska" last="Hopfner">Franziska Hopfner</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Neurology, University Hospital Schleswig Holstein, Kiel, Germany.</nlm:affiliation>
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<author><name sortKey="Muller, Stefanie H" sort="Muller, Stefanie H" uniqKey="Muller S" first="Stefanie H" last="Müller">Stefanie H. Müller</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Mutations in HTRA2 are not a common cause of familial classic ET.</title>
<author><name sortKey="Hopfner, Franziska" sort="Hopfner, Franziska" uniqKey="Hopfner F" first="Franziska" last="Hopfner">Franziska Hopfner</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Neurology, University Hospital Schleswig Holstein, Kiel, Germany.</nlm:affiliation>
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<author><name sortKey="Lorenz, Delia" sort="Lorenz, Delia" uniqKey="Lorenz D" first="Delia" last="Lorenz">Delia Lorenz</name>
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<author><name sortKey="Appenzeller, Silke" sort="Appenzeller, Silke" uniqKey="Appenzeller S" first="Silke" last="Appenzeller">Silke Appenzeller</name>
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<author><name sortKey="Klebe, Stephan" sort="Klebe, Stephan" uniqKey="Klebe S" first="Stephan" last="Klebe">Stephan Klebe</name>
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<author><name sortKey="Deuschl, Gunther" sort="Deuschl, Gunther" uniqKey="Deuschl G" first="Günther" last="Deuschl">Günther Deuschl</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<tree><country name="Allemagne"><region name="Schleswig-Holstein"><name sortKey="Hopfner, Franziska" sort="Hopfner, Franziska" uniqKey="Hopfner F" first="Franziska" last="Hopfner">Franziska Hopfner</name>
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<name sortKey="Appenzeller, Silke" sort="Appenzeller, Silke" uniqKey="Appenzeller S" first="Silke" last="Appenzeller">Silke Appenzeller</name>
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<name sortKey="Klebe, Stephan" sort="Klebe, Stephan" uniqKey="Klebe S" first="Stephan" last="Klebe">Stephan Klebe</name>
<name sortKey="Kuhlenb Umer, Gregor" sort="Kuhlenb Umer, Gregor" uniqKey="Kuhlenb Umer G" first="Gregor" last="Kuhlenb Umer">Gregor Kuhlenb Umer</name>
<name sortKey="Lorenz, Delia" sort="Lorenz, Delia" uniqKey="Lorenz D" first="Delia" last="Lorenz">Delia Lorenz</name>
<name sortKey="Muller, Stefanie H" sort="Muller, Stefanie H" uniqKey="Muller S" first="Stefanie H" last="Müller">Stefanie H. Müller</name>
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Movement Disorders (revue)

Mutations in HTRA2 are not a common cause of familial classic ET.

Mutations in HTRA2 are not a common cause of familial classic ET.

Source :

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.