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Search Results - Hartig, Monika B.
Search Results - Hartig, Monika B.
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Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
by
Hartig, Monika B.
,
Iuso, Arcangela
,
Haack, Tobias
,
Kmiec, Tomasz
,
Jurkiewicz, Elzbieta
,
Heim, Katharina
,
Roeber, Sigrun
,
Tarabin, Victoria
,
Dusi, Sabrina
,
Krajewska-Walasek, Malgorzata
,
Jozwiak, Sergiusz
,
Hempel, Maja
,
Winkelmann, Juliane
,
Elstner, Matthias
,
Oexle, Konrad
,
Klopstock, Thomas
,
Mueller-Felber, Wolfgang
,
Gasser, Thomas
,
Trenkwalder, Claudia
,
Tiranti, Valeria
,
Kretzschmar, Hans
,
Schmitz, Gerd
,
Strom, Tim M.
,
Meitinger, Thomas
,
Prokisch, Holger
Published in
American journal of human genetics
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Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation
by
Hartig, Monika B.
,
Hörtnagel, Konstanze
,
Garavaglia, Barbara
,
Zorzi, Giovanna
,
Kmiec, Tomasz
,
Klopstock, Thomas
,
Rostasy, Kevin
,
Svetel, Marina
,
Kostic, Vladimir S.
,
Schuelke, Markus
,
Botz, Evelyn
,
Weindl, Adolf
,
Novakovic, Ivana
,
Nardocci, Nardo
,
Prokisch, Holger
,
Meitinger, Thomas
Published in
Annals of neurology
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Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy
by
Haack, Tobias B.
,
Ignatius, Erika
,
Calvo-Garrido, Javier
,
Iuso, Arcangela
,
Isohanni, Pirjo
,
Maffezzini, Camilla
,
Lönnqvist, Tuula
,
Suomalainen, Anu
,
Gorza, Matteo
,
Kremer, Laura S.
,
Graf, Elisabeth
,
Hartig, Monika
,
Berutti, Riccardo
,
Paucar, Martin
,
Svenningsson, Per
,
Stranneheim, Henrik
,
Brandberg, Göran
,
Wedell, Anna
,
Kurian, Manju A.
,
Hayflick, Susan A.
,
Venco, Paola
,
Tiranti, Valeria
,
Strom, Tim M.
,
Dichgans, Martin
,
Horvath, Rita
,
Holinski-Feder, Elke
,
Freyer, Christoph
,
Meitinger, Thomas
,
Prokisch, Holger
,
Senderek, Jan
,
Wredenberg, Anna
,
Carroll, Christopher J.
,
Klopstock, Thomas
Published in
American journal of human genetics
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