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Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing

Overview of attention for article published in Orphanet Journal of Rare Diseases, October 2018
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Citations

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51 Mendeley
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Title
Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing
Published in
Orphanet Journal of Rare Diseases, October 2018
DOI 10.1186/s13023-018-0908-1
Pubmed ID
Authors

Sunita Bijarnia-Mahay, Johannes Häberle, Anil B. Jalan, Ratna Dua Puri, Sudha Kohli, Ketki Kudalkar, Véronique Rüfenacht, Deepti Gupta, Deepshikha Maurya, Jyotsna Verma, Yosuke Shigematsu, Seiji Yamaguchi, Renu Saxena, Ishwar C. Verma

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 51 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 51 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 8 16%
Researcher 7 14%
Other 3 6%
Student > Ph. D. Student 3 6%
Student > Master 3 6%
Other 5 10%
Unknown 22 43%
Readers by discipline Count As %
Medicine and Dentistry 10 20%
Biochemistry, Genetics and Molecular Biology 5 10%
Nursing and Health Professions 4 8%
Linguistics 1 2%
Pharmacology, Toxicology and Pharmaceutical Science 1 2%
Other 4 8%
Unknown 26 51%