Article

<i>In Silico</i> Analysis of <i>B3GALTL</i> Gene Reveling 13 Novel Mutations Associated with Peters’-plus syndrome

2020-03-23

Abstract excerpt

<h4>Background</h4> Peters’-plus syndrome is a rare autosomal recessive disorder, which is characterized by a specific malformation of the eye that includes corneal opaqueness and iridocorneal adhesions (Peters’ anomaly) along with other systemic manifestations. Furthermore, various researches report the association between B3GALTL gene and Peters’-plus syndrome. In the current work we aim to analyze the deleteri...

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Literature Corpus work: 71889dc2-2f41-5a4e-9f58-2f8a8cc55c7c
DOI: 10.1101/2020.03.21.000695

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