Pluto Bioinformatics

GSE143191: MMRN2 mutation underlies a rare form of autosomal-dominant laryngeal malformation

Bulk RNA sequencing

The aim of this study was to investigate the genetic basis and pathogenic mechanism of nonsyndromic laryngeal malformations, including disrupted thyroid cartilage structures and malformed vocal cords, in a four-generation family. SOURCE: Luo Guo (guoluo.gary@gmail.com) - Fudan University