Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family
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DOI: 10.1097/md.0000000000007138
Abstract: Introduction: Severe myopic anisometropia has been identified to have heritability, but the pathogenesis of anisometropia still remains obscure. Case description: Here, we presented a Chinese severe myopic anisometropia family with 5 members affected. Though using… read more here.
Keywords: anisometropia family; exome sequencing; severe myopic; myopic anisometropia ... See more keywords