Found: 3
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Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Identification of Six Novel Mutations in ZEB1 and Description of the Associated Phenotypes in Patients with Posterior Polymorphous Corneal Dystrophy 3.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12090
- By:
- Publication type:
- Article
Paraproteinemic keratopathy associated with monoclonal gammopathy of undetermined significance (MGUS): clinical findings in twelve patients including recurrence after keratoplasty.
- Published in:
- Acta Ophthalmologica (1755375X), 2019, v. 97, n. 7, p. e987, doi. 10.1111/aos.14123
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- Publication type:
- Article