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Identification of RNF13 as cause of recessively inherited ALS in a multi-case pedigree.
Khani, Marzieh; Nafissi, Shahriar; Shamshiri, Hosein; Moazzeni, Hamidreza; Taheri, Hanieh; Elahi, Elahe.
Afiliación
  • Khani M; School of Biology, College of Science, University of Tehran, Tehran, The Islamic Republic of Iran.
  • Nafissi S; Department of Neurology, Tehran University of Medical Sciences, Tehran, The Islamic Republic of Iran.
  • Shamshiri H; Department of Neurology, Tehran University of Medical Sciences, Tehran, The Islamic Republic of Iran.
  • Moazzeni H; School of Biology, College of Science, University of Tehran, Tehran, The Islamic Republic of Iran.
  • Taheri H; School of Biology, College of Science, University of Tehran, Tehran, The Islamic Republic of Iran.
  • Elahi E; School of Biology, College of Science, University of Tehran, Tehran, The Islamic Republic of Iran elaheelahi@ut.ac.ir elahe.elahi@gmail.com.
J Med Genet ; 2022 Jul 25.
Article en En | MEDLINE | ID: mdl-35879052
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: J Med Genet Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: J Med Genet Año: 2022 Tipo del documento: Article