Genetic screening of Russian Usher syndrome patients toward selection for gene therapy-Reference-Cited by-同舟云学术

Genetic screening of Russian Usher syndrome patients toward selection for gene therapy

Published:2018-10-25 Issue:6 Volume:39 Page:706-713
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Ivanova Marianna E.¹,Trubilin Vladimir N.²,Atarshchikov Dmitry S.³,Demchinsky Andrey M.⁴,Strelnikov Vladimir V.⁵,Tanas Alexander S.⁵,Orlova Olga M.²,Machalov Anton S.⁶,Overchenko Kira V.⁶,Markova Tatiana V.⁵,Golenkova Daria M.²,Anoshkin Kirill I.⁵,Volodin Ilya V.⁵,Zaletaev Dmitry V.⁷,Pulin Andrey A.⁸,Nadelyaeva Irina I.⁹,Kalinkin Alexey I.⁵⁷,Barh Debmalya¹⁰¹¹

Affiliation:

1. Oftalmic LLC, Moscow, Russia

2. Center of Ophthalmology, Federal Medical-Biological Agency State Research Center, Burnasyan, Moscow, Russia

3. Central Clinical Hospital under President Affairs, Moscow, Russia

4. Sensor-Tech Scientific and Industrial Laboratory, Moscow, Russia

5. Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russia

6. Surdology and Otoneurology Departments, Scientific and Clinical Center for Otorhinolaryngology of FMBA of Russia, Moscow, Russia

7. Laboratory of Medical Genetics, Institute of Molecular Medicine, I. M. Sechenov First Moscow State Medical University, Moscow, Russia

8. Laboratory of Cell Biology and Developmental Pathology, Federal State Budgetary Scientific Institution “Institute of General Pathology and Pathophysiology”, Moscow, Russia

9. Federal State Budget Institution of Higher Education, A.I. Yevdokimov Moscow State University of Medicine and Dentistry, The Ministry of Health Care of the Russia

10. Center for Genomics and Applied Gene Technology, Institute of Integrative Omics and Applied Biotechnology (IIOAB), Nonakuri, Purba Medinipur, West Bengal, India

11. Division of Bioinformatics and Computational Genomics, NITTE University Center for Science Education and Research (NUCSER), NITTE (Deemed to be University), Mangaluru, Karnataka, India

Funder

ANO “Sensor technology for deafblind”

Deaf-Blind Support Foundation

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2018.1532527

Reference28 articles.

1. Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children

3. Targeted next generation sequencing for molecular diagnosis of Usher syndrome

4. Development of a genotyping microarray for Usher syndrome

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