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Updated: Feb 4, 2026

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

Korbinian Maria Riedhammer1,2, Gloria Sarah Leszinski1, Stephanie Andres1,3

  • 1Institute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.

Movement Disorders : Official Journal of the Movement Disorder Society
|October 6, 2018
PubMed
Abstract

No abstract available in PubMed .

Keywords:
FITM2deafnessdystoniaexomehyperkeratosis

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