Literature DB >> 28095122

Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa.

Imen Habibi1,2,3,4, Ahmed Chebil2,5, Fedra Kort2,5, Daniel F Schorderet1,4,6, Leila El Matri2,5.   

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Year:  2017        PMID： 28095122     DOI： 10.1080/13816810.2016.1275020

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN： 1381-6810            Impact factor:   1.803


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  5 in total

1.  The genetics of rod-cone dystrophy in Arab countries: a systematic review.

Authors:  Hawraa Joumaa; Zamzam Mrad; Lama Jaffal; Christina Zeitz; Isabelle Audo; Said El Shamieh
Journal:  Eur J Hum Genet       Date:  2020-11-13       Impact factor: 5.351

2.  Genetic spectrum of retinal dystrophies in Tunisia.

Authors:  Imen Habibi; Yosra Falfoul; Ahmed Turki; Asma Hassairi; Khaled El Matri; Ahmed Chebil; Daniel F Schorderet; Leila El Matri
Journal:  Sci Rep       Date:  2020-07-08       Impact factor: 4.379

Review 3.  Genetic dissection of non-syndromic retinitis pigmentosa.

Authors:  Aarti Bhardwaj; Anshu Yadav; Manoj Yadav; Mukesh Tanwar
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

4.  Compound Heterozygous Mutations in ZNF408 in a Patient with a Late Onset Pigmentary Retinopathy and Relatively Preserved Central Retina.

Authors:  Jennifer B Nadelmann; Erin C O'Neil; Dale S Kim; Jane Juusola; Tomas S Aleman
Journal:  Doc Ophthalmol       Date:  2021-07-14       Impact factor: 2.379

5.  Modeling ZNF408-Associated FEVR in Zebrafish Results in Abnormal Retinal Vasculature.

Authors:  Dyah W Karjosukarso; Zaheer Ali; Theo A Peters; Jia Qi Cheng Zhang; Anita D M Hoogendoorn; Alejandro Garanto; Erwin van Wijk; Lasse D Jensen; Rob W J Collin
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-02-07       Impact factor: 4.799
  5 in total

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