Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings

Overview of attention for article published in Human Genomics, June 2020

Altmetric Badge

About this Attention Score

Average Attention Score compared to outputs of the same age
Average Attention Score compared to outputs of the same age and source

Mentioned by

twitter: 3 X users

Citations

dimensions_citation: 4 Dimensions

Readers on

mendeley: 5 Mendeley

Summary X Dimensions citations

So far, Altmetric has seen 3 X posts from 3 X users, with an upper bound of 3,222 followers.

RT @HumanGenomics: Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings | Human Genomics | Full Text…

Reply Repost Favourite

RT @HumanGenomics: Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings | Human Genomics | Full Text…

Reply Repost Favourite

Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings | Human Genomics | Full Text ⁦@vasilisyale⁩ ⁦@BioMedCentral⁩ https://t.co/M3PrN7Gw8H

Reply Repost Favourite

This page shows the most recent X posts that mention this research output.

Click here to find out how to access more activity.