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SZT2 mutation in a boy with intellectual disability, seizures and autistic features.
Kariminejad, Ariana; Yazdan, Hilda; Rahimian, Elham; Kalhor, Zahra; Fattahi, Zohreh; Zonooz, Mehrshid Faraji; Najmabadi, Hossein; Ashrafi, Mahmoudreza.
Afiliação
  • Kariminejad A; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran. Electronic address: arianakariminejad@yahoo.com.
  • Yazdan H; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran.
  • Rahimian E; Haghighat Medical Imaging Center, Tehran, Iran.
  • Kalhor Z; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Fattahi Z; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Zonooz MF; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran.
  • Najmabadi H; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Ashrafi M; Pediatrics Centre of Excellence, Department of Pediatric Neurology, Children's Medical Centre, Tehran University of Medical Sciences, Tehran, Iran.
Eur J Med Genet ; 62(9): 103556, 2019 Sep.
Article em En | MEDLINE | ID: mdl-30359774
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Convulsões / Transtorno Autístico / Deficiência Intelectual / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Convulsões / Transtorno Autístico / Deficiência Intelectual / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2019 Tipo de documento: Article