To report the clinical characteristics of a family with autosomal dominant retinitis pigmentosa caused by a proline-to-alanine mutation at codon 23 (Pro23Ala) of the rhodopsin gene and to compare this phenotype with that associated with the more common proline-to-histidine mutation at codon 23 (Pro23His).
Pharmacology, Toxicology and Pharmaceutical Science
1
4%
Nursing and Health Professions
1
4%
Other
2
7%
Unknown
5
19%
Attention Score in Context
Attention Score in Context
This research output has an Altmetric Attention Score of 5. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 11 July 2020.
All research outputs
#7,900,733
of 27,774,969 outputs
Outputs from Archives of Ophthalmology
#2
of 2 outputs
Outputs of similar age
#14,222
of 42,829 outputs
Outputs of similar age from Archives of Ophthalmology
#1
of 2 outputs
Altmetric has tracked 27,774,969 research outputs across all sources so far. This one has received more attention than most of these and is in the 71st percentile.
So far Altmetric has tracked 2 research outputs from this source. They receive a mean Attention Score of 2.4. This one scored the same or higher as 0 of them.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 42,829 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 66% of its contemporaries.
We're also able to compare this research output to 2 others from the same source and published within six weeks on either side of this one. This one has scored higher than all of them
