Fig. 11
From: Identification of a novel FGF3 variant and a new phenotype in three LAMM syndrome families
The c.137G > C mutation spanning the FGF3 gene have been associated with LAMM syndrome. The FGF3 protein contains one highly conserved fibroblast growth factor (FGF) domain (amino acids 44–181), a predicted signal peptide (SP, amino acids 1–17), and a predicted transmembrane domain (TM, amino acids 72–92)