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Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review

Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2019
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2 X users

Citations

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13 Dimensions

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30 Mendeley
Summary X Dimensions citations
So far, Dimensions has found 13 publications that cite this research output.

13

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