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Mandibuloacral dysplasia type B (MADB): a cohort of eight patients from Suriname with a homozygous founder mutation in ZMPSTE24 (FACE1), clinical diagnostic criteria and management guidelines

Overview of attention for article published in Orphanet Journal of Rare Diseases, December 2019
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Title
Mandibuloacral dysplasia type B (MADB): a cohort of eight patients from Suriname with a homozygous founder mutation in ZMPSTE24 (FACE1), clinical diagnostic criteria and management guidelines
Published in
Orphanet Journal of Rare Diseases, December 2019
DOI 10.1186/s13023-019-1269-0
Pubmed ID
Authors

M. M. Hitzert, S. N. van der Crabben, G. Baldewsingh, H. K. Ploos van Amstel, A. van den Wijngaard, C. M. A. van Ravenswaaij-Arts, C. W. R. Zijlmans

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 %
Unspecified 2 10%
Researcher 2 10%
Student > Postgraduate 2 10%
Student > Master 2 10%
Lecturer 1 5%
Other 3 15%
Unknown 8 40%
Readers by discipline Count As %
Medicine and Dentistry 5 25%
Biochemistry, Genetics and Molecular Biology 2 10%
Unspecified 2 10%
Chemistry 1 5%
Social Sciences 1 5%
Other 0 0%
Unknown 9 45%