Associated Papers
More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome.
Dhooge T et al.
Human Mutation, 2021
A role for repressive complexes and H3K9 di-methylation in PRDM5-associated brittle cornea syndrome.
Porter LF et al.
Human Molecular Genetics, 2015
Bruch's membrane abnormalities in PRDM5-related brittle cornea syndrome.
Porter LF et al.
Orphanet Journal of Rare Diseases, 2015
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