Your browser doesn't support javascript.
loading
Seizures, enamel defects and psychomotor developmental delay: The first patient with Kohlschütter-Tönz syndrome caused by a ROGDI-gene deletion.
Morscher, Raphael Johannes; Rauscher, Christian; Sperl, Wolfgang; Rittinger, Olaf.
Afiliación
  • Morscher RJ; Division of Clinical Genetics, Department of Pediatrics, Paracelsus Medical University, Salzburg, Austria; Division of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria. Electronic address: raphael.morscher@pmu.ac.at.
  • Rauscher C; Division of Clinical Genetics, Department of Pediatrics, Paracelsus Medical University, Salzburg, Austria.
  • Sperl W; Division of Clinical Genetics, Department of Pediatrics, Paracelsus Medical University, Salzburg, Austria.
  • Rittinger O; Division of Clinical Genetics, Department of Pediatrics, Paracelsus Medical University, Salzburg, Austria.
Seizure ; 50: 118-120, 2017 Aug.
Article en En | MEDLINE | ID: mdl-28651123

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Eliminación de Gen / Demencia / Epilepsia / Amelogénesis Imperfecta Límite: Child / Humans / Male Idioma: En Revista: Seizure Asunto de la revista: NEUROLOGIA Año: 2017 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Eliminación de Gen / Demencia / Epilepsia / Amelogénesis Imperfecta Límite: Child / Humans / Male Idioma: En Revista: Seizure Asunto de la revista: NEUROLOGIA Año: 2017 Tipo del documento: Article Pais de publicación: Reino Unido