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A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with charcot-... http://t.co/edVqGwy2 #haplotype #review
A Recurrent loss‐of‐function alanyl‐tRNA synthetase (AARS ) mutation in patients with charcot‐marie‐tooth disease type 2N (CMT2N)
Overview of attention for article published in Human Mutation, November 2011
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In the top 25% of all research outputs scored by Altmetric
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High Attention Score compared to outputs of the same age (88th percentile)
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High Attention Score compared to outputs of the same age and source (90th percentile)
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