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Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report

Overview of attention for article published in BMC Medical Genomics, January 2021
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Title
Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
Published in
BMC Medical Genomics, January 2021
DOI 10.1186/s12920-020-00861-3
Pubmed ID
Authors

Yahya Benbouchta, Imane Cherkaoui Jaouad, Habiba Tazi, Hamza Elorch, Mouna Ouhenach, Abdelali Zrhidri, Khalid Sadki, Abdelaziz Sefiani, Jaber Lyahyai, Amina Berraho

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Professor 1 20%
Student > Ph. D. Student 1 20%
Researcher 1 20%
Unknown 2 40%
Readers by discipline Count As %
Arts and Humanities 1 20%
Biochemistry, Genetics and Molecular Biology 1 20%
Unknown 3 60%