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Whole exome sequencing detects homozygosity for ABCA4 p.Arg602Trp missense mutation in a pediatric patient with rapidly progressive retinal dystrophy

Overview of attention for article published in BMC Medical Genomics, January 2014
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Title
Whole exome sequencing detects homozygosity for ABCA4 p.Arg602Trp missense mutation in a pediatric patient with rapidly progressive retinal dystrophy
Published in
BMC Medical Genomics, January 2014
DOI 10.1186/1471-2350-15-11
Pubmed ID
Authors

Maria Carolina Ortube, Samuel P Strom, Stanley F Nelson, Steven Nusinowitz, Ariadna Martinez, Michael B Gorin

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 27 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Hong Kong 1 4%
Spain 1 4%
Unknown 25 93%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 5 19%
Student > Ph. D. Student 5 19%
Student > Doctoral Student 2 7%
Student > Bachelor 2 7%
Researcher 2 7%
Other 5 19%
Unknown 6 22%
Readers by discipline Count As %
Agricultural and Biological Sciences 7 26%
Medicine and Dentistry 5 19%
Biochemistry, Genetics and Molecular Biology 4 15%
Psychology 1 4%
Nursing and Health Professions 1 4%
Other 2 7%
Unknown 7 26%