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A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA Splicing.
Ullah, Mukhtar; Rehman, Atta Ur; Folcher, Marc; Ullah, Adnan; Usman, Faisal; Rashid, Abdur; Khan, Bilal; Quinodoz, Mathieu; Ansar, Muhammad; Rivolta, Carlo.
Afiliação
  • Ullah M; Institute of Molecular and Clinical Ophthalmology Basel (IOB), Basel, Switzerland.
  • Rehman AU; Department of Ophthalmology, University of Basel, Basel, Switzerland.
  • Folcher M; Department of Zoology, Faculty of Biological and Health Sciences, Hazara University Mansehra, Mansehra, Pakistan.
  • Ullah A; Institute of Molecular and Clinical Ophthalmology Basel (IOB), Basel, Switzerland.
  • Usman F; Department of Ophthalmology, University of Basel, Basel, Switzerland.
  • Rashid A; Department of Zoology, Islamia College Peshawar, Peshawar, Pakistan.
  • Khan B; Department of Biotechnology and Genetic Engineering, Faculty of Biological and Health Sciences, Hazara University Mansehra, Mansehra, Pakistan.
  • Quinodoz M; Department of Higher Education, Archives and Libraries Peshawar, Peshawar, Pakistan.
  • Ansar M; Medical Teaching Institution Khyber Teaching Hospital Peshawar, Peshawar, Pakistan.
  • Rivolta C; Institute of Molecular and Clinical Ophthalmology Basel (IOB), Basel, Switzerland.
Ophthalmic Res ; 66(1): 878-884, 2023.
Article em En | MEDLINE | ID: mdl-37094557
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Retinose Pigmentar Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Retinose Pigmentar Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article