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Mendeley readers
Title |
Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype
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Published in |
BMC Medical Genomics, November 2012
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DOI | 10.1186/1471-2350-13-111 |
Pubmed ID | |
Authors |
Bridget A Fernandez, Jane S Green, Ford Bursey, Brendan Barrett, Andrée MacMillan, Sarah McColl, Sara Fernandez, Proton Rahman, Krista Mahoney, Sergio L Pereira, Stephen W Scherer, Kym M Boycott, Michael O Woods, FORGE Canada Consortium |
Mendeley readers
The data shown below were compiled from readership statistics for 32 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
Canada | 1 | 3% |
Unknown | 31 | 97% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Researcher | 7 | 22% |
Student > Ph. D. Student | 7 | 22% |
Student > Doctoral Student | 4 | 13% |
Student > Postgraduate | 3 | 9% |
Student > Bachelor | 2 | 6% |
Other | 5 | 16% |
Unknown | 4 | 13% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 13 | 41% |
Biochemistry, Genetics and Molecular Biology | 3 | 9% |
Agricultural and Biological Sciences | 3 | 9% |
Nursing and Health Professions | 2 | 6% |
Unspecified | 1 | 3% |
Other | 4 | 13% |
Unknown | 6 | 19% |