Sporadic and Familial Variants in NF1: An Explanation of the Wide Variability in Neurocognitive Phenotype?

Overview of attention for article published in Frontiers in Neurology, May 2020

Altmetric Badge

Mentioned by

twitter: 2 X users

Citations

dimensions_citation: 18 Dimensions

Readers on

mendeley: 66 Mendeley

Summary X Dimensions citations

So far, Altmetric has seen 2 X posts from 2 X users, with an upper bound of 12,435 followers.

RT @FrontNeurol: New Research: Sporadic and Familial Variants in NF1: An Explanation of the Wide Variability in Neurocognitive Phenotype?:…

08 May 2020

Reply Repost Favourite

New Research: Sporadic and Familial Variants in NF1: An Explanation of the Wide Variability in Neurocognitive Phenotype?: Background: Cognitive impairment is the most common neurological manifestation in NF1 and occurs in 30–70% of NF1 cases.… https://t.co

07 May 2020

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.