Cone Dystrophy/Cone-Rod Dystrophy
Inherited Retinal Disease, Page: 169-173
2022
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Book Chapter Description
Cone dystrophy is a rare genetic retinal disorder characterized by primary cone degeneration and secondary rod involvement, with a variable fundus appearance. The loss of cones leads to predominant symptoms such as decreased visual acuity, color vision defects and day blindness. Cone dystrophies are genetically heterogeneous and can be inherited by autosomal recessive, autosomal dominant or X-linked recessive patterns.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85160496933&origin=inward; http://dx.doi.org/10.1007/978-981-16-7337-5_10; https://link.springer.com/10.1007/978-981-16-7337-5_10; https://dx.doi.org/10.1007/978-981-16-7337-5_10; https://link.springer.com/chapter/10.1007/978-981-16-7337-5_10
Springer Science and Business Media LLC
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