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Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment.
Bahena, Paulina; Daftarian, Narsis; Maroofian, Reza; Linares, Paola; Villalobos, Daniel; Mirrahimi, Mehraban; Rad, Aboulfazl; Doll, Julia; Hofrichter, Michaela A H; Koparir, Asuman; Röder, Tabea; Han, Seungbin; Sabbaghi, Hamideh; Ahmadieh, Hamid; Behboudi, Hassan; Villanueva-Mendoza, Cristina; Cortés-Gonzalez, Vianney; Zamora-Ortiz, Rocio; Kohl, Susanne; Kuehlewein, Laura; Darvish, Hossein; Alehabib, Elham; Arenas-Sordo, Maria de la Luz; Suri, Fatemeh; Vona, Barbara; Haaf, Thomas.
Afiliação
  • Bahena P; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany.
  • Daftarian N; Ocular Tissue Engineering Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Maroofian R; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, UK.
  • Linares P; Universidad Nacional Autónoma de México, Mexico City, Mexico.
  • Villalobos D; Department of Bioinformatics, University of Würzburg, Würzburg, Germany.
  • Mirrahimi M; Ocular Tissue Engineering Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Rad A; Department of Otolaryngology-Head and Neck Surgery, Tübingen Hearing Research Centre, Eberhard Karls University Tübingen, 72076, Tübingen, Germany.
  • Doll J; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany.
  • Hofrichter MAH; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany.
  • Koparir A; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany.
  • Röder T; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany.
  • Han S; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany.
  • Sabbaghi H; Ophthalmic Epidemiology Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, No. 23, Paidarfard St., Boostan 9 St., Pasdaran Ave., Tehran, 1666673111, Iran.
  • Ahmadieh H; Ophthalmic Epidemiology Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, No. 23, Paidarfard St., Boostan 9 St., Pasdaran Ave., Tehran, 1666673111, Iran.
  • Behboudi H; Amiralmomenin Hospital, Eye Research Center, Guilan University of Medical Sciences, Rasht, Iran.
  • Villanueva-Mendoza C; Genetics Department, Asociación Para Evitar la Ceguera en México (APEC), Mexico City, Mexico.
  • Cortés-Gonzalez V; Genetics Department, Asociación Para Evitar la Ceguera en México (APEC), Mexico City, Mexico.
  • Zamora-Ortiz R; Ophthalmic Department, Instituto de Seguridad y Servicios sociales de los Trabajadores del Estado, Hospital de Alta Especialidad, Puebla, Mexico.
  • Kohl S; Centre for Ophthalmology, Institute for Ophthalmic Research, Eberhard Karls University Tübingen, Tübingen, Germany.
  • Kuehlewein L; Centre for Ophthalmology, Institute for Ophthalmic Research, Eberhard Karls University Tübingen, Tübingen, Germany.
  • Darvish H; University Eye Hospital, Centre for Ophthalmology, Eberhard Karls University Tübingen, Tübingen, Germany.
  • Alehabib E; Faculty of Medicine, Neuroscience Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
  • Arenas-Sordo ML; Student Research Committee, Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Suri F; Department of Genetics, National Institute of Rehabilitation Luis Guillermo Ibarra (INR), Mexico City, Mexico.
  • Vona B; Ophthalmic Epidemiology Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, No. 23, Paidarfard St., Boostan 9 St., Pasdaran Ave., Tehran, 1666673111, Iran. fatemehsuri@gmail.com.
  • Haaf T; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany. barbara.vona@uni-tuebingen.de.
Hum Genet ; 141(3-4): 785-803, 2022 Apr.
Article em En | MEDLINE | ID: mdl-34148116
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degeneração Retiniana / Síndromes de Usher Tipo de estudo: Diagnostic_studies / Prognostic_studies / Qualitative_research Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Hum Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degeneração Retiniana / Síndromes de Usher Tipo de estudo: Diagnostic_studies / Prognostic_studies / Qualitative_research Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Hum Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha