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A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report

Overview of attention for article published in BMC Neurology, October 2016
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Title
A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report
Published in
BMC Neurology, October 2016
DOI 10.1186/s12883-016-0716-y
Pubmed ID
Authors

Thashi Chang, Judith Cossins, David Beeson

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 %
Unknown 25 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 9 36%
Student > Doctoral Student 2 8%
Researcher 2 8%
Other 1 4%
Professor > Associate Professor 1 4%
Other 0 0%
Unknown 10 40%
Readers by discipline Count As %
Nursing and Health Professions 7 28%
Medicine and Dentistry 5 20%
Pharmacology, Toxicology and Pharmaceutical Science 1 4%
Social Sciences 1 4%
Neuroscience 1 4%
Other 0 0%
Unknown 10 40%