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EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum

Overview of attention for article published in Orphanet Journal of Rare Diseases, March 2021
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Title
EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum
Published in
Orphanet Journal of Rare Diseases, March 2021
DOI 10.1186/s13023-021-01744-1
Pubmed ID
Authors

Ulrike Hüffmeier, Cornelia Kraus, Miriam S. Reuter, Steffen Uebe, Mary-Alice Abbott, Syed A. Ahmed, Kristyn L. Rawson, Eileen Barr, Hong Li, Ange-Line Bruel, Laurence Faivre, Frédéric Tran Mau-Them, Christina Botti, Susan Brooks, Kaitlyn Burns, D. Isum Ward, Marina Dutra-Clarke, Julian A. Martinez-Agosto, Hane Lee, Stanley F. Nelson, Pia Zacher, Rami Abou Jamra, Chiara Klöckner, Julie McGaughran, Jürgen Kohlhase, Sarah Schuhmann, Ellen Moran, John Pappas, Annick Raas-Rothschild, Maria J. Guillen Sacoto, Lindsay B. Henderson, Timothy Blake Palculict, Sureni V. Mullegama, Houda Zghal Elloumi, Adi Reich, Samantha A. Schrier Vergano, Erica Wahl, André Reis, Christiane Zweier

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 20%
Unspecified 1 5%
Lecturer > Senior Lecturer 1 5%
Student > Bachelor 1 5%
Student > Doctoral Student 1 5%
Other 2 10%
Unknown 10 50%
Readers by discipline Count As %
Medicine and Dentistry 6 30%
Biochemistry, Genetics and Molecular Biology 3 15%
Philosophy 1 5%
Unspecified 1 5%
Agricultural and Biological Sciences 1 5%
Other 1 5%
Unknown 7 35%