Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Oct 2016

Liu Hongyan, Li Tao, Wang Hongdan, Guo Liangjie, Wu Dong, Xiao Hai, Guo Qiannan, Wang Tao

Abstract excerpt

OBJECTIVE: To analyze the clinical manifestations and mutation of MYH9 gene in a large Chinese family affected with MYH9-related thrombocytopenia. METHODS: After informed consent was obtained; clinical examination and history investigation was performed on 29 members of the family. DNA was extracted using a standard method, then exons 1 to 40 and their corresponding exon-intron junctions of the MYH9 gene were...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Asian People
Share to Exons

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family Health

Share to Molecular Motor Proteins

Share to Mutation, Missense

Share to Myosin Heavy Chains

Share to Sequence Homology, Amino Acid

Share to Thrombocytopenia

Source

Identifiers

PMID: 27577209
DOI: 10.3760/cma.j.issn.1003-9406.2016.05.010

Genes

MYH9

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia].PMID 27577209Read ↗

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

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

[Clinical features and gene analyses of six patients with MYH9-related disease].Semantic proximity Read ↗

[Identification of nonmuscle mysin heavy chain 9 gene mutation in a May-Hegglin anomaly family].Semantic proximity Read ↗

A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan.Semantic proximity Read ↗

[Nonmuscle myosin heavy chain 9 gene mutations related disease: a family report].Semantic proximity Read ↗

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

[Clinical and genetic features of seven children with MYH9-related disease].Semantic proximity Read ↗

Hereditary thrombocytopenia with familial novel mutation in MYH9 gene: A familial case report.Semantic proximity Read ↗

[Analysis of gene mutation in a family featuring autosomal dominant May-Hegglin anomaly].Semantic proximity Read ↗

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

MYH9-related inherited thrombocytopenia: the genetic spectrum, underlying mechanisms, clinical phenotypes, diagnosis, and management approachesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.