ScholarLens Back to search
2019•Experimental Eye ResearchRequires access

The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis

Ľubica Ďuďáková, Cerys J. Evans, Nikolas Pontikos, Nathaniel J. Hafford‐Tear, František Malinka, Pavlína Skalická, Aleš Hořínek, Francis L. Munier, Nathalie Voide, Pavel Studený, Lucia Vanikova, Tomáš Kuběna, Karla E. Rojas López, Alice E. Davidson, Alison J. Hardcastle, Stephen J. Tuft, Petra Lišková

Open publisher page 11 citations

Abstract

This record does not include an abstract. Use the full-text link above if available.

About this research paper

What this paper is about

An abstract is not available in the OpenAlex record for this paper.

Why it matters

OpenAlex reports 11 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Key concepts: Sanger sequencing, Massive parallel sequencing, Exome sequencing, Biology, Genetics, Proband, Exome, DNA sequencing

Related papers

Related paper 1Related paper 2Related paper 3
Back to paper searchBrowse research topicsOriginal source
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis — Research Paper | ScholarLens