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In Silico Analysis of B3GALTL Gene Reveling 13 Novel Mutations Associated with Peters’-plus syndrome
Autor:
Arwa A. Satti, Miysaa I. Abdelmageed, Abdelrahman H. Abdelmoneim, Nafisa M. Elfadol, Naseem S. Murshed, Abdelrafie M. Makhawi, Mujahed I. Mustafa
BackgroundPeters’-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 manifesta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::372a894a4eac4110eaaac56e3d5b5c1c
https://doi.org/10.1101/2020.03.21.000695
https://doi.org/10.1101/2020.03.21.000695
