Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability.
Smith CEL, Laugel-Haushalter V, Hany U, Best S, Taylor RL, Poulter JA, Wortmann SB, Feichtinger RG, Mayr JA, Al Bahlani S, Nikolopoulos G, Rigby A, Black GC, Watson CM, Mansour S, Inglehearn CF, Mighell AJ, Bloch-Zupan A; UK Inherited Retinal Disease Consortium, Genomics England Research Consortium.
Smith CEL, et al. Among authors: watson cm.
J Med Genet. 2024 Jun 20;61(7):689-698. doi: 10.1136/jmg-2023-109728.
J Med Genet. 2024.
PMID: 38458752
Free PMC article.