Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan

Overview of attention for article published in American Journal of Human Genetics, February 2013

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In the top 25% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (87th percentile)
Good Attention Score compared to outputs of the same age and source (71st percentile)

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twitter: 5 X users
patent: 1 patent

guideline: 2 clinical guideline sources

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mendeley: 115 Mendeley
citeulike: 2 CiteULike

So far, Altmetric has seen 7 X posts from 5 X users, with an upper bound of 14,317 followers.

Our paper B3GALNT2 mutations cause muscular dystrophy http://t.co/Zm2vOo2meX is one of @AJHGNews top 20 downloads!

Online today: B3GALNT2 mutations cause muscular dystrophy. http://t.co/2OC7bvGiSI #RDD

Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan. http://t.co/2HUmOsNXjv #Morpholino

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