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Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome
BMC Medical Genetics, August 2013
Ambroise Wonkam, Jean Jacques N Noubiap, Jason Bosch, Collet Dandara, Geneviève Bengono Toure
The data shown below were compiled from readership statistics for 33 Mendeley readers of this research output. Click here to see the associated Mendeley record.
|Readers by professional status||Count||As %|
|Student > Postgraduate||7||21%|
|Student > Bachelor||5||15%|
|Student > Doctoral Student||3||9%|
|Student > Ph. D. Student||3||9%|
|Readers by discipline||Count||As %|
|Agricultural and Biological Sciences||11||33%|
|Medicine and Dentistry||9||27%|
|Biochemistry, Genetics and Molecular Biology||4||12%|
|Nursing and Health Professions||2||6%|