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Fabry disease: Identification of 50 novel α-galactosidase A mutations causing the classic phenotype and three-dimensional structural analysis of 29 missense mutations

Overview of attention for article published in Human Genomics, March 2006
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Title
Fabry disease: Identification of 50 novel α-galactosidase A mutations causing the classic phenotype and three-dimensional structural analysis of 29 missense mutations
Published in
Human Genomics, March 2006
DOI 10.1186/1479-7364-2-5-297
Pubmed ID
Authors

Junaid Shabbeer, Makiko Yasuda, Stacy D Benson, Robert J Desnick

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 69 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 69 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 14 20%
Other 11 16%
Researcher 11 16%
Student > Ph. D. Student 7 10%
Student > Master 6 9%
Other 8 12%
Unknown 12 17%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 18 26%
Medicine and Dentistry 17 25%
Agricultural and Biological Sciences 16 23%
Economics, Econometrics and Finance 2 3%
Pharmacology, Toxicology and Pharmaceutical Science 1 1%
Other 4 6%
Unknown 11 16%