Variable phenotype of Knobloch syndrome due to biallelic...

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European Journal of Ophthalmology 2020 / 11

Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children

Levinger, Nadav, Hendler, Karen, Banin, Eyal, Hanany, Mor, Kimchi, Adva, Mechoulam, Hadas, Meiner, Vardiella, Parag, Yoav, Sharon, Dror, Macarov, Michal, Yahalom, Claudia
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Journal:
European Journal of Ophthalmology
DOI:
10.1177/1120672120977343
Date:
November, 2020
File:
PDF, 577 KB
2020
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