TRAPPC11 and congenital muscular dystrophy due to LMNA mutation: Most recently, Liang et al. reported a Chinese girl harboring a compound heterozygous c.2938G > A/c.661-1G > T mutations in TRAPPC11 presenting congenital muscular dystrophy, fatty liver, and infantile-onset cataract, demonstrating the broad spectrum of disease phenotypes arising from TRAPPC11 mutation in human [17].