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Article

KIF11 Mutation with Congenital Microcephaly and Chorioretinal Lacunae.

Ophthalmology. Retina - 1 Sept 2022

Shaikh Nawazish, Arora Bharat, Kumar Vinod

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PMID: 36084995
DOI: 10.1016/j.oret.2022.06.002

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KIF11 Mutation with Congenital Microcephaly and Chorioretinal Lacunae.PMID 36084995Read ↗

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Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)- The new lacunae: A case reportSemantic proximity Read ↗

KIF11-related Retinopathy with Microcephaly: Two Case Reports.Semantic proximity Read ↗

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Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation associated with KIF11 pathogenic variant: case report and genotype-phenotype correlation analysis.Semantic proximity Read ↗

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Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.Semantic proximity Read ↗

Total retinal detachment caused by a KIF11 mutation.Semantic proximity Read ↗

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