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Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family.

Clinical chemistry and laboratory medicine - 27 Sept 2021

Lian Xiaoqiang, Wang Yuxin, Gao Jie, Liu Heqiong, Hao Jihong, Kunishima Shinji

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PMID: 34013674
DOI: 10.1515/cclm-2021-0205

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Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family.PMID 34013674Read ↗

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Description of a novel mutation leading to MYH9-related disease.Semantic proximity Read ↗

A novel MYH9 variant in a Chinese patient with MYH9 related diseaseSemantic proximity Read ↗

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Early diagnosis improves the quality of life in MYH9 disorder.Semantic proximity Read ↗

[Gene analysis and clinical features of MYH9-related disease].Semantic proximity Read ↗

[Clinical manifestations and gene mutations of a Chinese family with MYH9-related syndrome].Semantic proximity Read ↗

[Identification of MYH9 gene mutation in a May-Hegglin anomaly family].Semantic proximity Read ↗

[Analysis of clinical phenotype and gene mutation characteristics of MYH9-related disorder].Semantic proximity Read ↗

Analysis of clinical manifestations, mutant gene and encoded protein in two Chinese MYH9-related disease families.Semantic proximity Read ↗

A Trp33Arg mutation at exon 1 of the MYH9 gene in a Korean patient with May-Hegglin anomaly.Semantic proximity Read ↗

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