Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family

Overview of attention for article published in Human Genetics, March 2014

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In the top 5% of all research outputs scored by Altmetric
Among the highest-scoring outputs from this source (#35 of 2,950)
High Attention Score compared to outputs of the same age (97th percentile)
High Attention Score compared to outputs of the same age and source (97th percentile)

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Researcher discovers two new genes linked to intellectual disability

Neuroscience, 01 Apr 2014

Researchers at the Centre for Addiction and Mental Health have discovered two new genes linked to...

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