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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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Extreme myopia in a family with a missense PAX6 mutation: extended phenotype
Vasily M Smirnov1,2, Patrick Calvas3,4,5, Isabelle Drumare1
1a Exploration of Vision and Neuro-ophthalmology Department , Lille University Hospital , Lille , France.
Ophthalmic Genetics
|December 29, 2018
Abstract
No abstract available in PubMed .
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