MFSD8 gene mutations; evidence for phenotypic heterogeneity-Reference-Cited by-同舟云学术

MFSD8 gene mutations; evidence for phenotypic heterogeneity

Published:2019-03-04 Issue:2 Volume:40 Page:141-145
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Zare-Abdollahi Davood¹,Bushehri Ata¹,Alavi Afagh¹,Dehghani Alireza²,Mousavi-Mirkala Mohammadreza³,Effati Jalil⁴,Miratashi Seyed Ali Mohammad⁵,Dehani Mohammad¹,Jamali Payman⁶,Khorram Khorshid Hamid Reza¹

Affiliation:

1. Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran

2. Department of Ophthalmology, Eye Research Center, Isfahan University of Medical Sciences, Isfahan, Iran

3. Department of Ophthalmology, Tabriz University of Medical Sciences, Tabriz, Iran

4. Meybod Genetic Research Center, State Welfare Organization of Yazd, Yazd, Iran

5. Department of Ophthalmology, Shahid Sadoughi University of Medical sciences, Yazd, Iran

6. Shahrood Genetic Counseling Center, Welfare Office, Semnan, Iran

Funder

State Welfare Organization of Iran

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2019.1592200

Reference29 articles.

1. Rod and Cone Photoreceptor Function in Patients with Cone Dystrophy

2. Genetische Ursachen erblicher Erkrankungen der Zapfen-Photorezeptoren

3. Clinical Course, Genetic Etiology, and Visual Outcome in Cone and Cone–Rod Dystrophy

4. Mutations in MFSD8, Encoding a Lysosomal Membrane Protein, Are Associated with Nonsyndromic Autosomal Recessive Macular Dystrophy

5. Cone rod dystrophies

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