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Academic Journal

[Study of GRIN2A mutation in epilepsy-aphasia spectrum disorders].

  • Authors : Qian P; Department of Pediatrics, Peking University First Hospital, Beijing 100034, China. .; Yang X

Subjects: Mutation*; Landau-Kleffner Syndrome/Landau-Kleffner Syndrome/Landau-Kleffner Syndrome/*genetics ; Receptors, N-Methyl-D-Aspartate/Receptors, N-Methyl-D-Aspartate/Receptors, N-Methyl-D-Aspartate/*genetics

  • Source: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2018 Jun 10; Vol. 35 (3), pp. 314-318.Publisher: Sichuan University Country of Publication: China NLM ID: 9425197 Publication Model: Print Cited Medium: Print

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  • 1-5 of  5 results for ""Landau-Kleffner Syndrome""