Your browser doesn't support javascript.
loading
Evaluation of point mutations in dystrophin gene in Iranian Duchenne and Becker muscular dystrophy patients: introducing three novel variants.
Haghshenas, Maryam; Akbari, Mohammad Taghi; Karizi, Shohreh Zare; Deilamani, Faravareh Khordadpoor; Nafissi, Shahriar; Salehi, Zivar.
Affiliation
  • Haghshenas M; Faculty of Sciences, Department of Biology, University of Guilan, Rasht 4199613776, Iran.mtakbari@modares.ac.ir.
J Genet ; 95(2): 325-9, 2016 Jun.
Article de En | MEDLINE | ID: mdl-27350676
Sujet(s)
Recherche sur Google
Ajouter à My VHL
Imprimer
XML
PubMed Links

Collection: 01-internacional Base de données: MEDLINE Sujet principal: Exons / Dystrophine / Mutation ponctuelle / Myopathie de Duchenne Type d'étude: Diagnostic_studies Limites: Adult / Child / Child, preschool / Humans / Male Langue: En Journal: J Genet Année: 2016 Type de document: Article Pays de publication: Inde
Recherche sur Google
Ajouter à My VHL
Imprimer
XML
PubMed Links

Collection: 01-internacional Base de données: MEDLINE Sujet principal: Exons / Dystrophine / Mutation ponctuelle / Myopathie de Duchenne Type d'étude: Diagnostic_studies Limites: Adult / Child / Child, preschool / Humans / Male Langue: En Journal: J Genet Année: 2016 Type de document: Article Pays de publication: Inde