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Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.
Caglayan, Ahmet Okay; Yaghouti, Kourosh; Kockaya, Tanyel; Kemer, Demet; Cankaya, Tufan; Ameziane, Najim; Cogulu, Ozgur; Coker, Mahmut; Yalcinkaya, Cengiz.
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  • Caglayan AO; Department of Medical Genetics, School of Medicine, Dokuz Eylul University, Izmir, Turkey.
  • Yaghouti K; Department of Radiology, Gayrettepe Florence Nightingale Hospital, Istanbul, Turkey.
  • Kockaya T; Department of Pediatrics, School of Medicine, Cerrahpasa University, Istanbul, Turkey.
  • Kemer D; Department of Medical Genetics, School of Medicine, Dokuz Eylul University, Izmir, Turkey.
  • Cankaya T; Department of Medical Genetics, School of Medicine, Dokuz Eylul University, Izmir, Turkey.
  • Ameziane N; Centogene AG, Rostock, Germany.
  • Cogulu O; Departments of Pediatrics and Medical Genetics, Ege University, Izmir, Turkey.
  • Coker M; Department of Pediatrics, Faculty of Medicine, Ege University, Izmir, Turkey.
  • Yalcinkaya C; Department of Neurology, School of Medicine, Cerrahpasa University, Istanbul, Turkey.
J Neurogenet ; 35(1): 23-28, 2021 Mar.
Article en En | MEDLINE | ID: mdl-33216650
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Ganglios Basales / Cerebelo / Proteínas de Unión al ADN / Mutación Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: J Neurogenet Año: 2021 Tipo del documento: Article País de afiliación: Turquía
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Ganglios Basales / Cerebelo / Proteínas de Unión al ADN / Mutación Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: J Neurogenet Año: 2021 Tipo del documento: Article País de afiliación: Turquía