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A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency

Overview of attention for article published in BMC Medical Genomics, December 2014
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Title
A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency
Published in
BMC Medical Genomics, December 2014
DOI 10.1186/s12881-014-0133-2
Pubmed ID
Authors

Muhammad Jameel, Joakim Klar, Muhammad Tariq, Abubakar Moawia, Naveed Altaf Malik, Syeda Seema Waseem, Uzma Abdullah, Tahir Naeem Khan, Raili Raininko, Shahid Mahmood Baig, Niklas Dahl

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 55 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 55 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 20%
Student > Postgraduate 6 11%
Student > Master 6 11%
Student > Ph. D. Student 5 9%
Student > Bachelor 3 5%
Other 11 20%
Unknown 13 24%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 11 20%
Agricultural and Biological Sciences 9 16%
Medicine and Dentistry 9 16%
Nursing and Health Professions 2 4%
Psychology 2 4%
Other 7 13%
Unknown 15 27%