Ophthalmic Manifestations of KIF11-Associated Microcephaly With or Without Chorioretinopathy, Lymphedema, or Intellectual Disability: A Case Report of a Novel Variant
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BACKGROUND Mutations in the kinesin family member 11 (KIF11) gene have been recently identified in several families worldwide. This gene plays a crucial role in cell division, chromosomal positioning, and separation. KIF11 mutations are associated clinically w... ...
