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FLASH GENE
Symbol FBN1 contributors: mct/npt/pgu - updated : 09-01-2018
HGNC name fibrillin 1 (Marfan syndrome)
HGNC id 3603
ANIMAL & CELL MODELS
  • decreased expression of Fbn1 during morphogenesis of the fetal diaphragm may disrupt mesenchymal cell proliferation, causing malformed muscle connective tissue (MCT) and thus resulting in diaphragmatic defects in the nitrofen-induced congenital diaphragmatic hernia (CDH) model