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HARVARD Citation
Levinger, N. et al. (2021). Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children. European journal of ophthalmology. 31 (6), pp. 3349-3354. [Online].
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Levinger, N. et al. (2021). Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children. European journal of ophthalmology. 31 (6), pp. 3349-3354. [Online].