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Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype

Overview of attention for article published in BMC Medical Genomics, November 2012
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32 Mendeley
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Title
Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype
Published in
BMC Medical Genomics, November 2012
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

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%