Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

Overview of attention for article published in American Journal of Medical Genetics. Part A, January 2015

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In the top 25% of all research outputs scored by Altmetric
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twitter: 3 X users
patent: 2 patents

wikipedia: 6 Wikipedia pages

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citeulike: 2 CiteULike

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So far, Altmetric has seen 3 X posts from 3 X users, with an upper bound of 2,872 followers.

Here’s a genetic disorder I’ll highlight from the Child Neurology Morning Conference: 🧠 Aicardi-Goutières Syndrome https://t.co/SVUr82hOl9 #neurotwitter

19 Jan 2023

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Read Dr. Sinha's latest research paper in the American Journal of Medical Genetics. https://t.co/Mb5suuPV0d @WalsallHcareNHS

09 Sep 2016

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Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C,... http://t.co/5JyEh1tSNN

16 Jan 2015

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