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Pendred Syndrome in a large consanguineous Brazilian family caused by a homozygous mutation in the SLC26A4 gene

Overview of attention for article published in Archives of Endocrinology and Metabolism, January 2009
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Title
Pendred Syndrome in a large consanguineous Brazilian family caused by a homozygous mutation in the SLC26A4 gene
Published in
Archives of Endocrinology and Metabolism, January 2009
DOI 10.1590/s0004-27302008000800015
Pubmed ID
Authors

Adriana Lofrano-Porto, Gustavo B. Barra, Paula P. Nascimento, Patrícia G. G. Costa, Érica C. Garcia, Rodrigo F. Vaz, Ana R. T. Batista, Ana C. R. de Freitas, Bruno L. B. Cherulli, Fayez Bahmad, Larissa G. Figueiredo, Francisco A. R. Neves, Luiz Augusto Casulari

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 36 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Portugal 1 3%
Unknown 35 97%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 22%
Student > Master 6 17%
Student > Ph. D. Student 4 11%
Professor > Associate Professor 4 11%
Student > Bachelor 2 6%
Other 9 25%
Unknown 3 8%
Readers by discipline Count As %
Medicine and Dentistry 15 42%
Agricultural and Biological Sciences 8 22%
Biochemistry, Genetics and Molecular Biology 3 8%
Business, Management and Accounting 1 3%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Other 3 8%
Unknown 5 14%