Pathology
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17 april 2019 19:04:43 |
| Tyrosinase (TYR) gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of oculocutaneous albinism (OCA) in Pakistani families (Eye) |
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| 66 viewsCategory: Neurology, Pathology |
 Visual Function Questionnaire as an outcome measure for homonymous hemianopia: subscales and supplementary questions, analysis from the VISION trial (Eye)Long-term natural history of idiopathic epiretinal membranes with good visual acuity (Eye) 
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