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Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patients.
Kunde, Stella-Amrei; Rademacher, Nils; Tzschach, Andreas; Wiedersberg, Eberhard; Ullmann, Reinhard; Kalscheuer, Vera M; Shoichet, Sarah A.
Affiliation
  • Kunde SA; Neuroscience Research Center, Charité CrossOver, Charité-Universitaetsmedizin Berlin, Campus Mitte, Charitéplatz 1, 10117 Berlin, Germany.
Hum Genet ; 132(4): 461-71, 2013 Apr.
Article in En | MEDLINE | ID: mdl-23329067

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Translocation, Genetic / Amino Acid Sequence / Sequence Deletion / Mitogen-Activated Protein Kinase 10 / Intellectual Disability Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Hum Genet Year: 2013 Document type: Article Affiliation country: Germany Country of publication: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Translocation, Genetic / Amino Acid Sequence / Sequence Deletion / Mitogen-Activated Protein Kinase 10 / Intellectual Disability Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Hum Genet Year: 2013 Document type: Article Affiliation country: Germany Country of publication: Germany