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Levinger N, Hendler K, Banin E, Hanany M, et al. Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in
children. Eur J Ophthalmol 2021;31:3349-3354.
PMID: 33238767
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 |
|
Levinger N, Hendler K, Banin E, Hanany M, et al. Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in
children. Eur J Ophthalmol 2021;31:3349-3354.
PMID: 33238767
|
|
|
|