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Novel mutation of FKBP10 in a pediatric patient with osteogenesis imperfecta type XI identified by clinical exome sequencing

Overview of attention for article published in The Application of Clinical Genetics, November 2017
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Mentioned by

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1 tweeter

Citations

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1 Dimensions

Readers on

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14 Mendeley
Title
Novel mutation of FKBP10 in a pediatric patient with osteogenesis imperfecta type XI identified by clinical exome sequencing
Published in
The Application of Clinical Genetics, November 2017
DOI 10.2147/tacg.s126277
Pubmed ID
Authors

Harvy Velasco Parra, Jessica Liliana Morales

Twitter Demographics

The data shown below were collected from the profile of 1 tweeter who shared this research output. Click here to find out more about how the information was compiled.

Mendeley readers

The data shown below were compiled from readership statistics for 14 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 14 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 3 21%
Student > Postgraduate 2 14%
Researcher 2 14%
Student > Master 2 14%
Student > Ph. D. Student 2 14%
Other 1 7%
Unknown 2 14%
Readers by discipline Count As %
Medicine and Dentistry 4 29%
Biochemistry, Genetics and Molecular Biology 3 21%
Engineering 2 14%
Psychology 1 7%
Pharmacology, Toxicology and Pharmaceutical Science 1 7%
Other 0 0%
Unknown 3 21%