Progressive degeneration of the retina in Loxl3 mutant mouse model of Stickler syndrome.
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DOI: 10.2139/ssrn.4207630
Abstract: Stickler syndrome is a multisystem collagenopathy with affected individuals exhibiting a high rate of ocular complications. Lysyl oxidase-like 3 (LOXL3) is a human disease gene candidate with a critical role in catalyzing collagen crosslinking. A… read more here.
Keywords: loxl3 mutant; loxl3; model stickler; mouse model ... See more keywords