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Identification of a new splice-acceptor mutation in HFM1 and functional analysis through molecular docking in nonobstructive azoospermia.
Saebnia, Neda; Ebrahimzadeh-Vesal, Reza; Haddad-Mashhadrizeh, Aliakbar; Gholampour-Faroji, Nazanin; Schinzel, Albert; Neshati, Zeinab; Azimi-Nezhad, Mohsen.
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  • Saebnia N; Department of Biology, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran.
  • Ebrahimzadeh-Vesal R; Non-Communicable Diseases Research Center, Neyshabur University of Medical Sciences, Neyshabur, Iran.
  • Haddad-Mashhadrizeh A; Industrial Biotechnology Research Group, Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad, Iran.
  • Gholampour-Faroji N; Biotechnology Department, Iranian Research Organization for Science and Technology (IROST), Tehran, Iran.
  • Schinzel A; Institute of Medical Genetics, University of Zurich, Zurich, Switzerland.
  • Neshati Z; Department of Biology, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran. neshati@um.ac.ir.
  • Azimi-Nezhad M; Novel Diagnostics and Therapeutics Research Group, Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad, Iran. neshati@um.ac.ir.
J Assist Reprod Genet ; 39(5): 1195-1203, 2022 May.
Article en En | MEDLINE | ID: mdl-35486194
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Azoospermia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Male Idioma: En Revista: J Assist Reprod Genet Asunto de la revista: GENETICA / MEDICINA REPRODUTIVA Año: 2022 Tipo del documento: Article País de afiliación: Irán
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Azoospermia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Male Idioma: En Revista: J Assist Reprod Genet Asunto de la revista: GENETICA / MEDICINA REPRODUTIVA Año: 2022 Tipo del documento: Article País de afiliación: Irán