https://adclinker-signal.com/i....ndex.php/erythropoie
The fibrillin-1 protein encoded by the FBN1 gene is a vital component of the lens zonules. Mutations in FBN1 will be the leading reasons for congenital EL and Marfan syndrome. Due to the complexity and individual heterogeneity of FBN1 gene mutations, the correlation between FBN1 mutation attributes and differing medical phenotypes stays confusing. Eight FBN1 mutations were identified in these families, of which three (c.5065G C, c.1600 T A, and c.2210G C
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