Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia

Overview of attention for article published in American Journal of Human Genetics, November 2015

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In the top 5% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (96th percentile)
Good Attention Score compared to outputs of the same age and source (76th percentile)

Mentioned by

news: 7 news outlets
blogs: 1 blog

twitter: 9 X users
facebook: 1 Facebook page

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mendeley: 64 Mendeley

So far, Altmetric has seen 8 news stories from 7 outlets.

MedUni Vienna researchers discover genetic cause of a rare disease

Health Medicinet, 15 Nov 2015

/ no comments Researchers at MedUni Vienna have discovered the genetic cause of a rare disease characterized by life-threatening…

MedUni Vienna researchers discover genetic cause of a rare disease

Health Medicinet, 15 Nov 2015

/ no comments Researchers at MedUni Vienna have discovered the genetic cause of a rare disease characterized by life-threatening…

MedUni Vienna researchers discover genetic cause of a rare disease

The Medical News, 15 Nov 2015

Published on November 15, 2015 at 6:49 AM Researchers at MedUni Vienna have discovered the genetic cause of a rare disease…

Health News - Genetic defect underlying a rare disease identified

Health Canal, 14 Nov 2015

(Vienna) Researchers at MedUni Vienna have discovered the genetic cause of a rare disease characterized by life-threatening "live…

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