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Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report

Overview of attention for article published in BMC Medical Genomics, September 2017
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Title
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report
Published in
BMC Medical Genomics, September 2017
DOI 10.1186/s12881-017-0463-y
Pubmed ID
Authors

Zsolt Bánfai, Kinga Hadzsiev, Endre Pál, Katalin Komlósi, Márton Melegh, László Balikó, Béla Melegh

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 35 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 35 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 6 17%
Student > Master 4 11%
Researcher 3 9%
Student > Bachelor 3 9%
Professor > Associate Professor 3 9%
Other 9 26%
Unknown 7 20%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 10 29%
Medicine and Dentistry 7 20%
Neuroscience 4 11%
Nursing and Health Professions 3 9%
Agricultural and Biological Sciences 2 6%
Other 1 3%
Unknown 8 23%