Korbinian Maria Riedhammer

Korbinian Maria Riedhammer

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Korbinian Maria Riedhammer

Korbinian Maria Riedhammer

Publications by authors named "Korbinian Maria Riedhammer"

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A De Novo Missense Variant in POU3F2 Identified in a Child with Global Developmental Delay.

Neuropediatrics 2018 12 10;49(6):401-404. Epub 2018 Sep 10.

Institute of Human Genetics, Technical University of Munich, Munich, Germany.

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http://dx.doi.org/10.1055/s-0038-1669926DOI Listing
December 2018

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