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NAA10 dysfunction with normal NatA-complex activity in a girl with non-syndromic ID and a de novo NAA10 p.(V111G) variant – a case report

Overview of attention for article published in BMC Medical Genomics, March 2018
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Title
NAA10 dysfunction with normal NatA-complex activity in a girl with non-syndromic ID and a de novo NAA10 p.(V111G) variant – a case report
Published in
BMC Medical Genomics, March 2018
DOI 10.1186/s12881-018-0559-z
Pubmed ID
Authors

Nina McTiernan, Svein Isungset Støve, Ingvild Aukrust, Marita Torrisen Mårli, Line M. Myklebust, Gunnar Houge, Thomas Arnesen

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 31 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 31 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 7 23%
Student > Doctoral Student 4 13%
Unspecified 2 6%
Researcher 2 6%
Lecturer 1 3%
Other 4 13%
Unknown 11 35%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 8 26%
Psychology 4 13%
Unspecified 2 6%
Neuroscience 2 6%
Agricultural and Biological Sciences 1 3%
Other 3 10%
Unknown 11 35%