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List of works by Graham E Holder

A clinical and molecular characterisation of CRB1-associated maculopathy ⬇️

scientific article published in February 2018

A phenotype-genotype correlation study of X-linked retinoschisis.

scientific article published on 28 February 2013

Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

scientific article published on 21 January 2017

Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis Pigmentosa

scientific article published on 5 January 2017

Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration

scientific article

Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in Humans

scientific article published on 07 November 2015

Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa ⬇️

scientific journal article

Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140.

scientific article

Pathognomonic (diagnostic) ERGs. A review and update.

scientific article published on January 2013

Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1.

scientific article published in September 2016

Retinal-detachment repair and vitreous-like-body reformation via a thermogelling polymer endotamponade

scientific article published on 08 April 2019

Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy ⬇️

scientific article published on June 2017

Unilateral pigmentary retinopathy: a retrospective case series

scientific article published on 31 December 2018

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