Gertrud Strobl-Wildemann

Gertrud Strobl-Wildemann

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Gertrud Strobl-Wildemann

Gertrud Strobl-Wildemann

Publications by authors named "Gertrud Strobl-Wildemann"

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First replication that biallelic variants in FITM2 cause a complex deafness-dystonia syndrome.

Mov Disord 2018 10 4;33(10):1665-1666. Epub 2018 Oct 4.

Institute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.

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http://doi.wiley.com/10.1002/mds.27481
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http://dx.doi.org/10.1002/mds.27481DOI Listing
October 2018

Next generation sequencing as a useful tool in the diagnostics of mosaicism in Alport syndrome.

Gene 2013 Sep 31;526(2):474-7. Epub 2013 May 31.

Center for Human Genetics and Laboratory Medicine Dr. Klein, Dr. Rost and Colleagues, Martinsried, Germany.

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http://dx.doi.org/10.1016/j.gene.2013.05.045DOI Listing
September 2013

Novel GDI1 mutation in a large family with nonsyndromic X-linked intellectual disability.

Am J Med Genet A 2011 Dec 14;155A(12):3067-70. Epub 2011 Oct 14.

Humangenetik Ulm MVZ, Ulm, Germany.

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http://dx.doi.org/10.1002/ajmg.a.34291DOI Listing
December 2011