Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment.
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| Title: | Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment. |
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| Authors: | 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.; University Eye Hospital, Centre for Ophthalmology, Eberhard Karls University Tübingen, Tübingen, Germany., Darvish H; Faculty of Medicine, Neuroscience Research Center, Golestan University of Medical Sciences, Gorgan, Iran., Alehabib E; Student Research Committee, Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Arenas-Sordo ML; Department of Genetics, National Institute of Rehabilitation Luis Guillermo Ibarra (INR), Mexico City, Mexico., Suri F; 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., Vona B; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany. barbara.vona@uni-tuebingen.de.; Department of Otolaryngology-Head and Neck Surgery, Tübingen Hearing Research Centre, Eberhard Karls University Tübingen, 72076, Tübingen, Germany. barbara.vona@uni-tuebingen.de., Haaf T; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany. thomas.haaf@uni-wuerzburg.de. |
| Source: | Human genetics [Hum Genet] 2022 Apr; Vol. 141 (3-4), pp. 785-803. Date of Electronic Publication: 2021 Jun 20. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1432-1203 |
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| DOI: | 10.1007/s00439-021-02303-1 |
