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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.
Afiliação
  • 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 em En | MEDLINE | ID: mdl-33216650
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Gânglios da Base / Cerebelo / Proteínas de Ligação a DNA / Mutação Tipo de estudo: Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: J Neurogenet Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Gânglios da Base / Cerebelo / Proteínas de Ligação a DNA / Mutação Tipo de estudo: Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: J Neurogenet Ano de publicação: 2021 Tipo de documento: Article