A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case report

Overview of attention for article published in BMC Neurology, January 2023

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: 3 Dimensions

Readers on

mendeley: 11 Mendeley

Summary X Dimensions citations

So far, Altmetric has seen 4 X posts from 3 X users, with an upper bound of 16,224 followers.

The case consisting of variant in the NEUORG1 gene was published in highly coveted @BioMedCentral #BMCNeurology journal. This is first family from India and only the fourth family worldwide. https://t.co/HMyGs2qSq1

16 Feb 2024

Reply Repost Favourite

RT @PaulWhiteleyPhD: A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype:…

19 Jan 2023

Reply Repost Favourite

RT @PaulWhiteleyPhD: A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype:…

17 Jan 2023

Reply Repost Favourite

You can read the paper 👇 https://t.co/HMyGs2rqfz

16 Jan 2023

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.