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Genetic research on Nance-Horan syndrome caused by a novel mutation in the NHS gene.

Gene - 15 May 2024

Yu Xuelin, Zhao Yueyue, Yang Zhenghua, Chen Xing, Kang Gangjing

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Identifiers

PMID: 38286268
DOI: 10.1016/j.gene.2024.148223

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Related research

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Genetic research on Nance-Horan syndrome caused by a novel mutation in the NHS gene.PMID 38286268Read ↗

[Identification of a novel variant of NHS gene underlying Nance-Horan syndrome].Semantic proximity Read ↗

New mutations in the NHS gene in Nance-Horan Syndrome families from the Netherlands.Semantic proximity Read ↗

Great clinical variability of Nance Horan syndrome due to deleterious NHS mutations in two unrelated Spanish families.Semantic proximity Read ↗

Identification of three novel NHS mutations in families with Nance-Horan syndrome.Semantic proximity Read ↗

[Clinical and genetic characterization of three families with Nance-Horan syndrome caused by NHS gene mutations].Semantic proximity Read ↗

A Novel Frameshift Mutation in The NHS Gene Causes Nance-Horan Syndrome in a Chinese FamilySemantic proximity Read ↗

A novel NHS mutation causes Nance-Horan Syndrome in a Chinese family.Semantic proximity Read ↗

A Turkish family with Nance-Horan Syndrome due to a novel mutation.Semantic proximity Read ↗

Identification of a novel NHS mutation in a Chinese family with Nance-Horan syndrome.Semantic proximity Read ↗

Erratum to: Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencingSemantic proximity Read ↗

Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing.Semantic proximity Read ↗

Nance-Horan Syndrome: Characterization of dental, clinical and molecular features in three new familiesSemantic proximity Read ↗

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