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Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred.
Sadeghian, Ladan; Tabatabaiefar, Mohammad Amin; Fattahi, Najmeh; Pourreza, Mohammad Reza; Tahmasebi, Parisa; Alavi, Zahra; Hashemzadeh Chaleshtori, Morteza.
Affiliation
  • Sadeghian L; Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
  • Tabatabaiefar MA; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Fattahi N; Cilinical Biochemistry Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
  • Pourreza MR; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Tahmasebi P; Department of Biology, Faculty of Sciences, Ilam University, Ilam, Iran.
  • Alavi Z; Department of Genetics, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran.
  • Hashemzadeh Chaleshtori M; Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran. Electronic address: mchalesh@yahoo.com.
Int J Pediatr Otorhinolaryngol ; 124: 99-105, 2019 Sep.
Article de En | MEDLINE | ID: mdl-31176026
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Perte d'audition / Protéines membranaires Type d'étude: Guideline / Prognostic_studies Limites: Female / Humans / Male Pays/Région comme sujet: Asia Langue: En Journal: Int J Pediatr Otorhinolaryngol Année: 2019 Type de document: Article Pays d'affiliation: Iran Pays de publication: Irlande
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Perte d'audition / Protéines membranaires Type d'étude: Guideline / Prognostic_studies Limites: Female / Humans / Male Pays/Région comme sujet: Asia Langue: En Journal: Int J Pediatr Otorhinolaryngol Année: 2019 Type de document: Article Pays d'affiliation: Iran Pays de publication: Irlande