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PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran.
Jafarzadeh Esfehani, Reza; Eslahi, Atieh; Beiraghi Toosi, Mehran; Sadr-Nabavi, Ariane; Kerachian, Mohammad Amin; Asl Mohajeri, Mahsa Sadat; Farjami, Mahsa; Alizade, Farzaneh; Mojarrad, Majid.
Afiliação
  • Jafarzadeh Esfehani R; Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Eslahi A; Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Beiraghi Toosi M; Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Sadr-Nabavi A; Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Kerachian MA; Department of Paediatric Neurology, Ghaem Medical Centre, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad.
  • Asl Mohajeri MS; Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Farjami M; Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Alizade F; Iranian Academic Center for Education, Culture and Research, (ACECR), Mashhad, Iran.
  • Mojarrad M; Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Iran J Basic Med Sci ; 24(9): 1190-1195, 2021 Sep.
Article em En | MEDLINE | ID: mdl-35083005
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Iran J Basic Med Sci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Irã
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Iran J Basic Med Sci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Irã