Entries of Elstner, Matthias on the publication server
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2011
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 and Prokisch, Holger
(2011)
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation.
The American Journal of Human Genetics 89 (4), pp. 543-550.
Fulltext not available.
, 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 and Prokisch, Holger
(2011)
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation.
The American Journal of Human Genetics 89 (4), pp. 543-550.
Fulltext not available.