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Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

Overview of attention for article published in Molecular Cytogenetics, September 2015
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Title
Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?
Published in
Molecular Cytogenetics, September 2015
DOI 10.1186/s13039-015-0178-8
Pubmed ID
Authors

Julia K. Ehret, Hartmut Engels, Kirsten Cremer, Jessica Becker, Johannes P. Zimmermann, Eva Wohlleber, Ute Grasshoff, Eva Rossier, Michael Bonin, Elisabeth Mangold, Andrea Bevot, Stefanie Schön, Stefanie Heilmann-Heimbach, Nicola Dennert, Michèle Mathieu-Dramard, Elodie Lacaze, Ghislaine Plessis, Alain de Broca, Guillaume Jedraszak, Benno Röthlisberger, Peter Miny, Isabel Filges, Andreas Dufke, Joris Andrieux, Jennifer A. Lee, Alexander M. Zink

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 40 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 40 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 7 18%
Unspecified 6 15%
Researcher 5 13%
Student > Bachelor 4 10%
Student > Master 4 10%
Other 7 18%
Unknown 7 18%
Readers by discipline Count As %
Medicine and Dentistry 10 25%
Unspecified 6 15%
Biochemistry, Genetics and Molecular Biology 5 13%
Agricultural and Biological Sciences 3 8%
Computer Science 2 5%
Other 7 18%
Unknown 7 18%