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Subtle mutations in the SMN1 gene in Chinese patients with SMA: p.Arg288Met mutation causing SMN1 transcript exclusion of exon7

Overview of attention for article published in BMC Medical Genomics, September 2012
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Title
Subtle mutations in the SMN1 gene in Chinese patients with SMA: p.Arg288Met mutation causing SMN1 transcript exclusion of exon7
Published in
BMC Medical Genomics, September 2012
DOI 10.1186/1471-2350-13-86
Pubmed ID
Authors

Qu Yu-jin, Du Juan, Li Er-zhen, Bai Jin-li, Jin Yu-wei, Wang Hong, Song Fang

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 25 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Korea, Republic of 1 4%
Canada 1 4%
Unknown 23 92%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 20%
Student > Bachelor 3 12%
Other 2 8%
Student > Master 2 8%
Researcher 2 8%
Other 3 12%
Unknown 8 32%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 20%
Medicine and Dentistry 4 16%
Agricultural and Biological Sciences 4 16%
Mathematics 1 4%
Neuroscience 1 4%
Other 1 4%
Unknown 9 36%