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Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature

Overview of attention for article published in BMC Medical Genomics, September 2018
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Title
Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature
Published in
BMC Medical Genomics, September 2018
DOI 10.1186/s12881-018-0678-6
Pubmed ID
Authors

Siying Lin, Gaurav V. Harlalka, Abdul Hameed, Hadia Moattar Reham, Muhammad Yasin, Noor Muhammad, Saadullah Khan, Emma L. Baple, Andrew H. Crosby, Shamim Saleha

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 27 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 27 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 8 30%
Student > Doctoral Student 3 11%
Student > Bachelor 3 11%
Student > Ph. D. Student 3 11%
Researcher 2 7%
Other 2 7%
Unknown 6 22%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 26%
Medicine and Dentistry 7 26%
Nursing and Health Professions 2 7%
Business, Management and Accounting 1 4%
Sports and Recreations 1 4%
Other 1 4%
Unknown 8 30%