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Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations

Overview of attention for article published in Orphanet Journal of Rare Diseases, October 2015
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  • Above-average Attention Score compared to outputs of the same age (56th percentile)
  • Average Attention Score compared to outputs of the same age and source

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4 X users

Citations

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44 Dimensions

Readers on

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74 Mendeley
Summary X Dimensions citations
So far, Dimensions has found 44 publications that cite this research output.

44

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