Clinical feature and waveform in infantile nystagmus syndrome in children with FRMD7 gene mutations-Reference-Cited by-同舟云学术

Clinical feature and waveform in infantile nystagmus syndrome in children with FRMD7 gene mutations

Published:2017-06-14 Issue:7 Volume:60 Page:707-713
ISSN:1674-7305
Container-title:Science China Life Sciences
language:en
Short-container-title:Sci. China Life Sci.

Author:

Bai Dayong,Shi Wei,Qi Zhan,Li Wei,Wei Aihua,Cui Yanhui,Li Cheng,Li Li

Publisher

Springer Science and Business Media LLC

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Biochemistry, Genetics and Molecular Biology

Link

http://link.springer.com/article/10.1007/s11427-017-9089-5/fulltext.html

Reference22 articles.

1. Abadi, R.V. (1991). Sensory and Motor Aspects of Congenital Nystagmus. (North Holland: Elsevier science publishers RV), pp. 249–256.

2. Abadi, R.V., and Dickinson, C.M. (1986). Waveform characteristics in congenital nystagmus. Doc Ophthalmol 64, 153–167.

3. Ahmedbegovic, P.M1., Alikadic-Husovic, A., Griševic, S., Pašalic, A., Pidro, A., Ratkovic, M., Bohac, M., Gabric, N., and Gojak, R. (2016). Efficacy and safety of iris-supported phakic lenses (Verisyse) for treating moderately high myopia. Med Glas (Zenica) 13, 25–30.

4. Dell’Osso, L.F., and Daroff, R.B. (1975). Congenital nystagmus waveforms and foveation strategy. Doc Ophthalmo 139, 155–182.

5. Denis, D., Girard, N., Toesca, E., Zanin, E., Gambarelli, N., Lebranchu, P., and Mancini, J. (2010). Apport de l’IRM dans les nystagmus congénitaux. J Français d’Ophtalmologie 33, 189–205.

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Truncated FRMD7 proteins in congenital Nystagmus: novel frameshift mutations and proteasomal pathway implications;BMC Medical Genomics;2024-01-26

2. Exposure to SARS-CoV-2 and Infantile Diseases;Global Medical Genetics;2023-05-02

3. X-linked FRMD7 gene mutation in idiopathic congenital nystagmus and its role in eye movement: A case report and literature review;Frontiers in Ophthalmology;2023-03-06

4. Genotype-Phenotype Analysis and Mutation Spectrum in a Cohort of Chinese Patients With Congenital Nystagmus;Frontiers in Cell and Developmental Biology;2021-02-19

5. Le bilan étiologique d’un nystagmus chez l’enfant;Journal Français d'Ophtalmologie;2018-11