A novel 5 bp homozygous deletion mutation in ASPH gene associates with Traboulsi syndrome.

Ophthalmic Genet

b Department of Genetics , Dr. G. Venkataswamy Eye Research Institute, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai , India.

Published: April 2019

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Source
http://dx.doi.org/10.1080/13816810.2019.1605390DOI Listing

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