A zebrafish model of crim1 loss of function has small and misshapen lenses with dysregulated clic4 and fgf1b expression
IntroductionHeterozygous deletions predicting haploinsufficiency for the Cysteine Rich Motor Neuron 1 (CRIM1) gene have been identified in two families with macrophthalmia, colobomatous, with microcornea (MACOM), an autosomal dominant trait. Crim1 encodes a type I transmembrane protein that is expre...
Autors principals: | , , , , , , , , , , , , , |
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Format: | Article |
Idioma: | English |
Publicat: |
Frontiers Media S.A.
2025-03-01
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Col·lecció: | Frontiers in Cell and Developmental Biology |
Matèries: | |
Accés en línia: | https://www.frontiersin.org/articles/10.3389/fcell.2025.1522094/full |