Literature DB >> 29518905

Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68.

Karin W Littink1, Patricia T Y Stappers2, Frans C C Riemslag3,4, Herman E Talsma5,6, Maria M van Genderen7, Frans P M Cremers8,9, Rob W J Collin10,11, L Ingeborgh van den Born12.   

Abstract

The authors wish to make the following correction to this paper [1]. [...].

Entities:  

Year:  2018        PMID： 29518905      PMCID： PMC5867866          DOI： 10.3390/genes9030145

Source DB:  PubMed          Journal:  Genes (Basel)        ISSN： 2073-4425            Impact factor:   4.096


The authors wish to make the following correction to this paper [1]. Due to mislabeling, replace: with The authors would like to apologize for any inconvenience caused to the readers by these changes.
  1 in total

1.  Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome.

Authors:  Karin W Littink; Patricia T Y Stappers; Frans C C Riemslag; Herman E Talsma; Maria M van Genderen; Frans P M Cremers; Rob W J Collin; L Ingeborgh van den Born
Journal:  Genes (Basel)       Date:  2018-01-30       Impact factor: 4.096
  1 in total
  8 in total

1.  Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosa.

Authors:  Mohammed E El-Asrag; Marta Corton; Martin McKibbin; Almudena Avila-Fernandez; Moin D Mohamed; Fiona Blanco-Kelly; Carmel Toomes; Chris F Inglehearn; Carmen Ayuso; Manir Ali
Journal:  Mol Vis       Date:  2022-05-17       Impact factor: 2.711

2.  ENHANCED S-CONE SYNDROME: VISUAL FUNCTION, CROSS-SECTIONAL IMAGING, AND CELLULAR STRUCTURE WITH ADAPTIVE OPTICS OPHTHALMOSCOPY.

Authors:  Michael J Ammar; Kurt T Scavelli; Katherine E Uyhazi; Emma C Bedoukian; Leona W Serrano; Ilaina D Edelstein; Grace Vergilio; Robert F Cooper; Jessica I W Morgan; Priyanka Kumar; Tomas S Aleman
Journal:  Retin Cases Brief Rep       Date:  2021-11-01

Review 3.  Patient derived stem cells for discovery and validation of novel pathogenic variants in inherited retinal disease.

Authors:  Nathaniel K Mullin; Andrew P Voigt; Jessica A Cooke; Laura R Bohrer; Erin R Burnight; Edwin M Stone; Robert F Mullins; Budd A Tucker
Journal:  Prog Retin Eye Res       Date:  2020-10-29       Impact factor: 21.198

4.  Enhanced S-cone syndrome: Clinical spectrum in Indian population.

Authors:  Anmol Naik; Dhanashree Ratra; Aniruddha Banerjee; Daleena Dalan; Sourabh Jandyal; Girish Rao; Parveen Sen; Muna Bhende; V Jayaprakash; Pradeep Susvar; Jaydeep Walinjkar; Chetan Rao
Journal:  Indian J Ophthalmol       Date:  2019-04       Impact factor: 1.848

5.  Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization.

Authors:  Matteo Di Scipio; Erika Tavares; Shriya Deshmukh; Isabelle Audo; Kit Green-Sanderson; Yuliya Zubak; Fayçal Zine-Eddine; Alexander Pearson; Anjali Vig; Chen Yu Tang; Antonio Mollica; Jonathan Karas; Anupreet Tumber; Caberry W Yu; Gail Billingsley; Michael D Wilson; Christina Zeitz; Elise Héon; Ajoy Vincent
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-08-03       Impact factor: 4.799

Review 6.  Zebrafish Models of Photoreceptor Dysfunction and Degeneration.

Authors:  Nicole C L Noel; Ian M MacDonald; W Ted Allison
Journal:  Biomolecules       Date:  2021-01-09

7.  Novel Pathogenic Sequence Variants in NR2E3 and Clinical Findings in Three Patients.

Authors:  Saoud Al-Khuzaei; Suzanne Broadgate; Stephanie Halford; Jasleen K Jolly; Morag Shanks; Penny Clouston; Susan M Downes
Journal:  Genes (Basel)       Date:  2020-10-29       Impact factor: 4.096

8.  NRL-/- gene edited human embryonic stem cells generate rod-deficient retinal organoids enriched in S-cone-like photoreceptors.

Authors:  Elisa Cuevas; Daniel L Holder; Ashwak H Alshehri; Julie Tréguier; Jörn Lakowski; Jane C Sowden
Journal:  Stem Cells       Date:  2021-01-19       Impact factor: 5.845
  8 in total

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