A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions
Page 1 of 1
A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions
Oliver VF, van Bysterveldt KA, Cadzow M, Steger B, Romano V, Markie D, Hewitt AW, Mackey DA, Willoughby CE, Sherwin T, Crosier PS, McGhee CN, Vincent AL. A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions. Ophthalmol. 2016;[Epub ahead of print] doi:10.1016/j.ophtha.2015.12.008
Similar topics
» Induced IL-10 Splice Altering Approach to Antiviral Drug Discovery
» A Recurrent CEP120 Mutation in Jeune Asphyxiating Thoracic Dystrophy Expands the Role of Centriolar Proteins in Skeletal Ciliopathies
» Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome
» A mild neurofibromatosis type 1 phenotype produced by the combination of the benign nature of a leaky NF1-splice mutation and the presence of a complex mosaicism
» Absence of heartbeat in the Xenopus tropicalis mutation muzak is caused by a nonsense mutation in cardiac myosin myh6
» A Recurrent CEP120 Mutation in Jeune Asphyxiating Thoracic Dystrophy Expands the Role of Centriolar Proteins in Skeletal Ciliopathies
» Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome
» A mild neurofibromatosis type 1 phenotype produced by the combination of the benign nature of a leaky NF1-splice mutation and the presence of a complex mosaicism
» Absence of heartbeat in the Xenopus tropicalis mutation muzak is caused by a nonsense mutation in cardiac myosin myh6
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum