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

A novel 5 bp homozygous deletion mutation in ASPH gene associates with Traboulsi syndrome. Ophthalmic Genet. 2019 Apr 23;:1-3 Authors: Chandran P, Chermakani P, Venkataraman P, Thilagar SP, Raman GV, Sundaresan P PMID: 31012784 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/31012784?dopt=Abstract

Source: Ophthalmic Genetics - April 25, 2019 Category: Opthalmology Tags: Ophthalmic Genet Source Type: research

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