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Novel DCC variants in congenital mirror movements and evaluation of disease-associated missense variants.
Bierhals, Tatjana; Korenke, Georg Christoph; Baethmann, Martina; Marín, Laura López; Staudt, Martin; Kutsche, Kerstin.
Affiliation
  • Bierhals T; Institut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
  • Korenke GC; Zentrum für Kinder- und Jugendmedizin, Neuropädiatrie, Klinikum Oldenburg GmbH, Oldenburg, Germany.
  • Baethmann M; Klinik für Kinder- und Jugendmedizin, Klinikum Dritter Orden, München, Germany.
  • Marín LL; Hospital Infantil Univesitario Niño Jesús, Paediatric Neurology Department, Madrid, Spain.
  • Staudt M; Klinik für Neuropädiatrie und Neurorehabilitation, Epilepsiezentrum für Kinder und Jugendliche, Schön-Klinik Vogtareuth, Vogtareuth, Germany.
  • Kutsche K; Institut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany. Electronic address: kkutsche@uke.de.
Eur J Med Genet ; 61(6): 329-334, 2018 Jun.
Article in En | MEDLINE | ID: mdl-29366874
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / DCC Receptor / Movement Disorders Type of study: Guideline / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: Alemania Country of publication: Países Bajos
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / DCC Receptor / Movement Disorders Type of study: Guideline / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: Alemania Country of publication: Países Bajos