Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction

Overview of attention for article published in BMC Medical Genomics, May 2018

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So far, Altmetric has seen 2 X posts from 2 X users, with an upper bound of 668 followers.

Over the past few years I split my time between #SensoryTreat and #Genoox. This innovative paper brings these two loves of mine together, showing a #genetic basis for #SPD https://t.co/czLMqRXCOB

Burden of de novo mutations and inherited rare single nucleotide variants in children with senso... https://t.co/zAfrDYqHHG #bmcmedgenomics

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