A Zebrafish Model for a Rare Genetic Disease Reveals a Conserved Role for FBXL3 in the Circadian Clock System.
Confino S, Dor T, Tovin A, Wexler Y, Ben-Moshe Livne Z, Kolker M, Pisanty O, Park SK, Geyer N, Reiter J, Edvardson S, Mor-Shaked H, Elpeleg O, Vallone D, Appelbaum L, Foulkes NS, Gothilf Y.
Confino S, et al.
Int J Mol Sci. 2022 Feb 21;23(4):2373. doi: 10.3390/ijms23042373.
Int J Mol Sci. 2022.
PMID: 35216494
Free PMC article.
By exome sequencing, we have identified a FBXL3 mutation in patients with syndromic developmental delay accompanied by morphological abnormalities and intellectual disability, albeit with a normal sleep pattern. We have investigated the function of FBXL3 in the zebr …
By exome sequencing, we have identified a FBXL3 mutation in patients with syndromic developmental delay accompanied by morphological …