Your browser doesn't support javascript.
loading
A comprehensive overview of SMN and NAIP copy numbers in Iranian SMA patients.
Savad, Shahram; Ashrafi, Mahmoud Reza; Samadaian, Niusha; Heidari, Morteza; Modarressi, Mohammad-Hossein; Zamani, Gholamreza; Amidi, Saloomeh; Younesi, Sarang; Amin, Mohammad Mahdi Taheri; Saadati, Pourandokht; Ronagh, Alireza; Ardakani, Hossein Shojaaldini; Eslami, Solat; Ghafouri-Fard, Soudeh.
Afiliação
  • Savad S; Genome-Nilou Laboratory, Tehran, Iran. Shahram.savad@yahoo.com.
  • Ashrafi MR; Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Ataxia Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Samadaian N; Department of Pediatrics Center, Growth and Development Research Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Heidari M; Genome-Nilou Laboratory, Tehran, Iran.
  • Modarressi MH; Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Ataxia Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Zamani G; Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Amidi S; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Younesi S; Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Amin MMT; Genome-Nilou Laboratory, Tehran, Iran.
  • Saadati P; Prenatal Screening Department, Nilou Laboratory, Tehran, Iran.
  • Ronagh A; Prenatal Screening Department, Nilou Laboratory, Tehran, Iran.
  • Ardakani HS; Prenatal Screening Department, Nilou Laboratory, Tehran, Iran.
  • Eslami S; Department of Pediatrics Neurologists, Shahid Bahonar Hospital, Alborz University of Medical Sciences, Karaj, Iran.
  • Ghafouri-Fard S; Department of Medical, Faculty of Medical Sciences, Alborz University of Medical Sciences, Karaj, Iran.
Sci Rep ; 13(1): 3202, 2023 02 24.
Article em En | MEDLINE | ID: mdl-36828874
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Variações do Número de Cópias de DNA Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Sci Rep Ano de publicação: 2023 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: Atrofia Muscular Espinal / Variações do Número de Cópias de DNA Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Sci Rep Ano de publicação: 2023 Tipo de documento: Article