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Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects
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A zebrafish model for Bruck syndrome caused by PLOD2 mutations
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Characterization of a col1a1a haploinsufficient zebrafish model for Osteogenesis Imperfecta type I
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A zebrafish model for Bruck Syndrome caused by PLOD2 mutations
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Characterization of a COL1A1A haploinsufficient zebrafish model for Osteogenesis Imperfecta type I