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Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome

Overview of attention for article published in BMC Medical Genomics, August 2013
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34 Mendeley
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Title
Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome
Published in
BMC Medical Genomics, August 2013
DOI 10.1186/1471-2350-14-81
Pubmed ID
Authors

Ambroise Wonkam, Jean Jacques N Noubiap, Jason Bosch, Collet Dandara, Geneviève Bengono Toure

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 34 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
India 1 3%
Unknown 33 97%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 7 21%
Student > Bachelor 5 15%
Researcher 4 12%
Student > Doctoral Student 3 9%
Student > Ph. D. Student 3 9%
Other 7 21%
Unknown 5 15%
Readers by discipline Count As %
Agricultural and Biological Sciences 11 32%
Medicine and Dentistry 9 26%
Biochemistry, Genetics and Molecular Biology 4 12%
Nursing and Health Professions 2 6%
Psychology 1 3%
Other 2 6%
Unknown 5 15%