Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2019

Altmetric Badge

About this Attention Score

Good Attention Score compared to outputs of the same age (66th percentile)
Good Attention Score compared to outputs of the same age and source (68th percentile)

So far, Altmetric has seen 9 X posts from 7 X users, with an upper bound of 4,843 followers.

RT @ingentium_hd: Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry. https://t.co/O7KqddqehF

Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry. https://t.co/O7KqddqehF

RT @gracescience: New paper on #NGLY1 deficiency @ojrarediseases! So grateful to NGLY1 families for their participation in the registry and…

RT @emcahan: Our collab btwn @StanfordOrthop1 & @gracescience addressing ortho manifestations of NGLY1 deficiency is live! Hopefully a step…

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

Click here to find out how to access more activity, including 5 additional X posts.