A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C.

Jensen, Lars R; Bartenschlager, Heinz; Rujirabanjerd, Sinitdhorn; Tzschach, Andreas; Nümann, Astrid; Janecke, Andreas R; Spörle, Ralf; Stricker, Sigmar; Raynaud, Martine; Nelson, John; Hackett, Anna; Fryns, Jean-Pierre; Chelly, Jamel; de Brouwer, Arjan Pm; Hamel, Ben; Gecz, Jozef; Ropers, Hans-Hilger; Kuss, Andreas W

Jensen, Lars R; Bartenschlager, Heinz; Rujirabanjerd, Sinitdhorn; Tzschach, Andreas; Nümann, Astrid; Janecke, Andreas R; Spörle, Ralf; Stricker, Sigmar; Raynaud, Martine; Nelson, John; Hackett, Anna; Fryns, Jean-Pierre; Chelly, Jamel; de Brouwer, Arjan Pm; Hamel, Ben; Gecz, Jozef; Ropers, Hans-Hilger; Kuss, Andreas W.

Affiliation

Jensen LR; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany. kuss_a@molgen.mpg.de.

Pathogenetics ; 3(1): 2, 2010 Feb 02.

Article in En | MEDLINE | ID: mdl-20181063

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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Pathogenetics Year: 2010 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido

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