Found: 7
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A previously unidentified deletion in G protein-coupled receptor 143 causing X-linked congenital nystagmus in a Chinese family.
- Published in:
- 2016
- By:
- Publication type:
- journal article
A novel splice donor site mutation in EPHA2 caused congenital cataract in a Chinese family.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Comparing myopic error in patients with basic and convergence insufficiency intermittent exotropia in China.
- Published in:
- BMC Ophthalmology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12886-023-03043-8
- By:
- Publication type:
- Article
Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation.
- Published in:
- Journal of Human Genetics, 2007, v. 52, n. 6, p. 565, doi. 10.1007/s10038-007-0152-3
- By:
- Publication type:
- Article
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.
- Published in:
- Nature Genetics, 2005, v. 37, n. 7, p. 733, doi. 10.1038/ng1585
- By:
- Publication type:
- Article
Modified Posterior Scleral Reinforcement as a Treatment for High Myopia in Children and Its Therapeutic Effect.
- Published in:
- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/5185780
- By:
- Publication type:
- Article
The critical role of m<sup>6</sup>A methylation in the pathogenesis of Graves' ophthalmopathy.
- Published in:
- Eye & Vision, 2020, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40662-020-00221-3
- By:
- Publication type:
- Article