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Genetic Analysis of Forty MLPA-Negative Duchenne Muscular Dystrophy Patients by Whole-Exome Sequencing.
Zamani, Gholam Reza; Mohammadi, Mohammad Farid; Tavasoli, Ali Reza; Ashrafi, Mahmoud Reza; Hosseinpour, Sareh; Ghabeli, Homa; Pourbakhtyaran, Elham; Haghighi, Roya; Hosseiny, Seyyed Mohammad Mahdi; Mohammadi, Pouria; Heidari, Morteza.
Afiliação
  • Zamani GR; Department of Pediatric Neurology, Pediatrics Center of Excellence, Children's Medical Center, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Mohammadi MF; Department of Cell and Molecular Sciences, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.
  • Tavasoli AR; Department of Pediatric Neurology, Pediatrics Center of Excellence, Children's Medical Center, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Ashrafi MR; Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, USA.
  • Hosseinpour S; Department of Pediatric Neurology, Pediatrics Center of Excellence, Children's Medical Center, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Ghabeli H; Department of Pediatric Neurology, Vali-E-Asr Hospital, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
  • Pourbakhtyaran E; Department of Pediatric Neurology, Pediatrics Center of Excellence, Children's Medical Center, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Haghighi R; Department of Pediatric Neurology, Pediatrics Center of Excellence, Children's Medical Center, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Hosseiny SMM; Department of Pediatric Neurology, Pediatrics Center of Excellence, Children's Medical Center, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Mohammadi P; Department of Pediatric Neurology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
  • Heidari M; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Postal Code, Jalah-Al Ahmad Hwy, 14117-1316, Tehran, Iran. Pouria.mohammaditmu@gmail.com.
J Mol Neurosci ; 72(5): 1098-1107, 2022 May.
Article em En | MEDLINE | ID: mdl-35218518
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofia Muscular de Duchenne Tipo de estudo: Risk_factors_studies Limite: Female / Humans País/Região como assunto: Asia Idioma: En Revista: J Mol Neurosci Assunto da revista: BIOLOGIA MOLECULAR / NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Irã País de publicação: Estados Unidos
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofia Muscular de Duchenne Tipo de estudo: Risk_factors_studies Limite: Female / Humans País/Região como assunto: Asia Idioma: En Revista: J Mol Neurosci Assunto da revista: BIOLOGIA MOLECULAR / NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Irã País de publicação: Estados Unidos