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Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy.
Chapi, Marjan; Sabbaghi, Hamideh; Suri, Fatemeh; Alehabib, Elham; Rahimi-Aliabadi, Simin; Jamali, Faezeh; Jamshidi, Javad; Emamalizadeh, Babak; Darvish, Hossein; Mirrahimi, Mehraban; Ahmadieh, Hamid; Daftarian, Narsis.
Afiliação
  • Chapi M; a Department of Medical Genetics , School of Medicine, Shahid Beheshti University of Medical Sciences , Tehran , Iran.
  • Sabbaghi H; b Ophthalmic Research Center , Shahid Beheshti University of Medical Sciences , Tehran , Iran.
  • Suri F; b Ophthalmic Research Center , Shahid Beheshti University of Medical Sciences , Tehran , Iran.
  • Alehabib E; a Department of Medical Genetics , School of Medicine, Shahid Beheshti University of Medical Sciences , Tehran , Iran.
  • Rahimi-Aliabadi S; a Department of Medical Genetics , School of Medicine, Shahid Beheshti University of Medical Sciences , Tehran , Iran.
  • Jamali F; a Department of Medical Genetics , School of Medicine, Shahid Beheshti University of Medical Sciences , Tehran , Iran.
  • Jamshidi J; c Department of Psychology , University of New South Wales and Neuroscience Research Australia , Sydney , NSW , Australia.
  • Emamalizadeh B; d Noncommunicable Diseases Research Center , Fasa University of Medical Sciences , Fasa , Iran.
  • Darvish H; e Department of Medical Genetics, Faculty of Medicine , Tabriz University of Medical Sciences , Tabriz , Iran.
  • Mirrahimi M; f Cancer Research Center , Semnan University of Medical Sciences , Semnan , Iran.
  • Ahmadieh H; g Department of Medical Genetics , Semnan University of Medical Sciences , Semnan , Iran.
  • Daftarian N; h Ocular Tissue Engineering Research Center , Shahid Beheshti University of Medical Sciences , Tehran , Iran.
Ophthalmic Genet ; 40(3): 259-266, 2019 06.
Article em En | MEDLINE | ID: mdl-31215831
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transativadores / Proteínas de Homeodomínio / Polimorfismo de Nucleotídeo Único / Distrofias de Cones e Bastonetes / Genes Dominantes Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transativadores / Proteínas de Homeodomínio / Polimorfismo de Nucleotídeo Único / Distrofias de Cones e Bastonetes / Genes Dominantes Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article